Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome X:67545150 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960074

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8538, 2010_April_001_014_AR_313700_0038

This variation has 15 HGVS names - click the plus to show

X:g.67545150G>A
ENST00000504326.2:c.4G>A
ENSP00000421155.1:p.Glu2Lys
ENST00000613054.1:c.4G>A
ENSP00000479013.1:p.Glu2Lys
ENST00000396044.4:c.4G>A
ENSP00000379359.3:p.Glu2Lys
ENST00000374690.4:c.4G>A
ENSP00000363822.3:p.Glu2Lys
ENST00000514029.2:c.4G>A
ENSP00000425199.1:p.Glu2Lys
ENST00000612452.1:c.-567G>A
ENST00000612010.1:c.4G>A
ENSP00000482407.1:p.Glu2Lys
ENST00000513847.2:n.331G>A

Variation displays