Canonical Allele Identifier: CA408634595

Gene: SNTA1

Linked Data

• dbSNP Id: rs1433264223
• gnomAD v2: 20-32031345-A-G
• gnomAD v4: 20-33443539-A-G
• MyVariant Identifiers: chr20:g.32031345A>G (hg19) ; chr20:g.33443539A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443539A>G , CM000682.2:g.33443539A>G	GRCh38
NC_000020.10:g.32031345A>G , CM000682.1:g.32031345A>G	GRCh37
NC_000020.9:g.31495006A>G	NCBI36
NG_011622.1:g.5354T>C , LRG_332:g.5354T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.82T>C MANE Select	ENSP00000217381.2:p.Trp28Arg
ENST00000217381.2:c.82T>C	ENSP00000217381.2:p.Trp28Arg
NM_003098.2:c.82T>C , LRG_332t1:c.82T>C	NP_003089.1:p.Trp28Arg
XM_005260517.1:c.82T>C	XP_005260574.1:p.Trp28Arg
XM_011529007.1:c.82T>C	XP_011527309.1:p.Trp28Arg
XM_011529008.1:c.82T>C	XP_011527310.1:p.Trp28Arg
XR_936612.1:n.315T>C
NM_003098.3:c.82T>C MANE Select	NP_003089.1:p.Trp28Arg