Canonical Allele Identifier: CA313279142
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs983131823

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443568C>G , CM000682.2:g.33443568C>G GRCh38
NC_000020.10:g.32031374C>G , CM000682.1:g.32031374C>G GRCh37
NC_000020.9:g.31495035C>G NCBI36
NG_011622.1:g.5325G>C , LRG_332:g.5325G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.53G>C MANE Select ENSP00000217381.2:p.Gly18Ala
ENST00000217381.2:c.53G>C ENSP00000217381.2:p.Gly18Ala
NM_003098.2:c.53G>C , LRG_332t1:c.53G>C NP_003089.1:p.Gly18Ala
XM_005260517.1:c.53G>C XP_005260574.1:p.Gly18Ala
XM_011529007.1:c.53G>C XP_011527309.1:p.Gly18Ala
XM_011529008.1:c.53G>C XP_011527310.1:p.Gly18Ala
XR_936612.1:n.286G>C
NM_003098.3:c.53G>C MANE Select NP_003089.1:p.Gly18Ala