Original source

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

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

Chromosome 8:22163458 (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.22163458C>A
ENST00000521315.3:c.347C>A
ENSP00000430410.1:p.Ala116Asp
ENST00000522109.3:c.347C>A
ENSP00000429496.1:p.Ala116Asp
ENST00000520605.3:c.188C>A
ENSP00000430266.1:p.Ala63Asp
ENST00000437090.4:c.347C>A
ENSP00000407931.2:p.Ala116Asp
ENST00000524255.3:c.188C>A
ENSP00000429552.1:p.Ala63Asp
ENST00000522630.2:n.146C>A
ENST00000318561.5:c.347C>A
ENSP00000316152.3:p.Ala116Asp
ENST00000523296.1:c.188C>A
ENSP00000429619.1:p.Ala63Asp

Variation displays