Original source

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

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

Chromosome 8:22020971 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 5085

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

8:g.22020971C>A
ENST00000521315.1:c.347C>A
ENSP00000430410.1:p.Ala116Asp
ENST00000522109.1:c.347C>A
ENSP00000429496.1:p.Ala116Asp
ENST00000520605.1:c.188C>A
ENSP00000430266.1:p.Ala63Asp
ENST00000437090.2:c.347C>A
ENSP00000407931.2:p.Ala116Asp
ENST00000524255.1:c.188C>A
ENSP00000429552.1:p.Ala63Asp
ENST00000522630.1:n.147C>A
ENST00000523296.1:c.188C>A
ENSP00000429619.1:p.Ala63Asp
ENST00000318561.3:c.347C>A
ENSP00000316152.3:p.Ala116Asp

Variation displays