Canonical Allele Identifier: CA635719651
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1338107775

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443787T>C , CM000682.2:g.33443787T>C GRCh38
NC_000020.10:g.32031593T>C , CM000682.1:g.32031593T>C GRCh37
NC_000020.9:g.31495254T>C NCBI36
NG_011622.1:g.5106A>G , LRG_332:g.5106A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.2:c.-167A>G ENSP00000217381.2:n.-167A>G
NM_003098.2:c.-167A>G , LRG_332t1:c.-167A>G NP_003089.1:n.-167A>G
XM_005260517.1:c.-167A>G XP_005260574.1:n.-167A>G
XM_011529007.1:c.-167A>G XP_011527309.1:n.-167A>G
XM_011529008.1:c.-167A>G XP_011527310.1:n.-167A>G
XR_936612.1:n.67A>G