Canonical Allele Identifier: CA408634742

Gene: SNTA1

Linked Data

• dbSNP Id: rs1419918481
• gnomAD v4: 20-33443579-C-G
• MyVariant Identifiers: chr20:g.32031385C>G (hg19) ; chr20:g.33443579C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443579C>G , CM000682.2:g.33443579C>G	GRCh38
NC_000020.10:g.32031385C>G , CM000682.1:g.32031385C>G	GRCh37
NC_000020.9:g.31495046C>G	NCBI36
NG_011622.1:g.5314G>C , LRG_332:g.5314G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.42G>C MANE Select	ENSP00000217381.2:p.Glu14Asp
ENST00000217381.2:c.42G>C	ENSP00000217381.2:p.Glu14Asp
NM_003098.2:c.42G>C , LRG_332t1:c.42G>C	NP_003089.1:p.Glu14Asp
XM_005260517.1:c.42G>C	XP_005260574.1:p.Glu14Asp
XM_011529007.1:c.42G>C	XP_011527309.1:p.Glu14Asp
XM_011529008.1:c.42G>C	XP_011527310.1:p.Glu14Asp
XR_936612.1:n.275G>C
NM_003098.3:c.42G>C MANE Select	NP_003089.1:p.Glu14Asp