Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 5:143281982 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021312

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_050_NR3C1_138040_0009, 2192

This variation has 16 HGVS names - click the plus to show

5:g.143281982A>C
ENST00000394464.3:c.2241T>G
ENSP00000377977.2:p.Ile747Met
ENST00000231509.4:c.2244T>G
ENSP00000231509.3:p.Ile748Met
ENST00000343796.3:c.2241T>G
ENSP00000343205.2:p.Ile747Met
ENST00000503201.1:c.2241T>G
ENSP00000427672.1:p.Ile747Met
ENST00000504572.2:c.2244T>G
ENSP00000422518.1:p.Ile748Met
ENST00000415690.3:c.2181+586T>G
ENST00000394466.3:c.2244T>G
ENSP00000377979.2:p.Ile748Met
ENST00000424646.3:c.2163T>G
ENSP00000405282.2:p.Ile721Met

Variation displays