Canonical Allele Identifier: CA408634639

Gene: SNTA1

Linked Data

• dbSNP Id: rs1234217932
• gnomAD v2: 20-32031356-C-T
• gnomAD v4: 20-33443550-C-T
• MyVariant Identifiers: chr20:g.32031356C>T (hg19) ; chr20:g.33443550C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443550C>T , CM000682.2:g.33443550C>T	GRCh38
NC_000020.10:g.32031356C>T , CM000682.1:g.32031356C>T	GRCh37
NC_000020.9:g.31495017C>T	NCBI36
NG_011622.1:g.5343G>A , LRG_332:g.5343G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.71G>A MANE Select	ENSP00000217381.2:p.Gly24Asp
ENST00000217381.2:c.71G>A	ENSP00000217381.2:p.Gly24Asp
NM_003098.2:c.71G>A , LRG_332t1:c.71G>A	NP_003089.1:p.Gly24Asp
XM_005260517.1:c.71G>A	XP_005260574.1:p.Gly24Asp
XM_011529007.1:c.71G>A	XP_011527309.1:p.Gly24Asp
XM_011529008.1:c.71G>A	XP_011527310.1:p.Gly24Asp
XR_936612.1:n.304G>A
NM_003098.3:c.71G>A MANE Select	NP_003089.1:p.Gly24Asp