Canonical Allele Identifier: CA408633454
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1990511120

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438919C>T , CM000682.2:g.33438919C>T GRCh38
NC_000020.10:g.32026725C>T , CM000682.1:g.32026725C>T GRCh37
NC_000020.9:g.31490386C>T NCBI36
NG_011622.1:g.9974G>A , LRG_332:g.9974G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.418G>A MANE Select ENSP00000217381.2:p.Gly140Arg
ENST00000217381.2:c.418G>A ENSP00000217381.2:p.Gly140Arg
NM_003098.2:c.418G>A , LRG_332t1:c.418G>A NP_003089.1:p.Gly140Arg
XM_005260517.1:c.418G>A XP_005260574.1:p.Gly140Arg
XM_011529007.1:c.418G>A XP_011527309.1:p.Gly140Arg
XM_011529008.1:c.418G>A XP_011527310.1:p.Gly140Arg
XR_936612.1:n.651G>A
XM_024451971.1:c.91G>A XP_024307739.1:p.Gly31Arg
NM_003098.3:c.418G>A MANE Select NP_003089.1:p.Gly140Arg