Canonical Allele Identifier: CA1017044253
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1990643678
gnomAD v3: 20-33443786-G-A
gnomAD v4: 20-33443786-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443786G>A , CM000682.2:g.33443786G>A GRCh38
NC_000020.10:g.32031592G>A , CM000682.1:g.32031592G>A GRCh37
NC_000020.9:g.31495253G>A NCBI36
NG_011622.1:g.5107C>T , LRG_332:g.5107C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.2:c.-166C>T ENSP00000217381.2:n.-166C>T
NM_003098.2:c.-166C>T , LRG_332t1:c.-166C>T NP_003089.1:n.-166C>T
XM_005260517.1:c.-166C>T XP_005260574.1:n.-166C>T
XM_011529007.1:c.-166C>T XP_011527309.1:n.-166C>T
XM_011529008.1:c.-166C>T XP_011527310.1:n.-166C>T
XR_936612.1:n.68C>T
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