Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 5:143310135 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM014593

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_053_NR3C1_138040_0013, 2196

This variation has 18 HGVS names - click the plus to show

5:g.143310135C>T
ENST00000394464.4:c.1430G>A
ENSP00000377977.2:p.Arg477His
ENST00000231509.5:c.1433G>A
ENSP00000231509.3:p.Arg478His
ENST00000504336.1:n.370G>A
ENST00000503201.1:c.1430G>A
ENSP00000427672.1:p.Arg477His
ENST00000504572.3:c.1433G>A
ENSP00000422518.1:p.Arg478His
ENST00000424646.4:c.1352G>A
ENSP00000405282.2:p.Arg451His
ENST00000343796.4:c.1430G>A
ENSP00000343205.2:p.Arg477His
ENST00000415690.4:c.1430G>A
ENSP00000387672.2:p.Arg477His
ENST00000394466.4:c.1433G>A
ENSP00000377979.2:p.Arg478His

Variation displays