Canonical Allele Identifier: CA2652478580
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443711G>A , CM000682.2:g.33443711G>A GRCh38
NC_000020.10:g.32031517G>A , CM000682.1:g.32031517G>A GRCh37
NC_000020.9:g.31495178G>A NCBI36
NG_011622.1:g.5182C>T , LRG_332:g.5182C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.3:c.-91C>T MANE Select ENSP00000217381.2:n.-91C>T
ENST00000217381.2:c.-91C>T ENSP00000217381.2:n.-91C>T
NM_003098.2:c.-91C>T , LRG_332t1:c.-91C>T NP_003089.1:n.-91C>T
XM_005260517.1:c.-91C>T XP_005260574.1:n.-91C>T
XM_011529007.1:c.-91C>T XP_011527309.1:n.-91C>T
XM_011529008.1:c.-91C>T XP_011527310.1:n.-91C>T
XR_936612.1:n.143C>T
NM_003098.3:c.-91C>T MANE Select NP_003089.1:n.-91C>T