Canonical Allele Identifier: CA2360755168
Gene: SNTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443801G= , CM000682.2:g.33443801G= GRCh38
NC_000020.10:g.32031607G= , CM000682.1:g.32031607G= GRCh37
NC_000020.9:g.31495268G= NCBI36
NG_011622.1:g.5092C= , LRG_332:g.5092C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.2:c.-181C= ENSP00000217381.2:n.-181C=
NM_003098.2:c.-181C= , LRG_332t1:c.-181C= NP_003089.1:n.-181C=
XM_005260517.1:c.-181C= XP_005260574.1:n.-181C=
XM_011529007.1:c.-181C= XP_011527309.1:n.-181C=
XM_011529008.1:c.-181C= XP_011527310.1:n.-181C=
XR_936612.1:n.53C=