Canonical Allele Identifier: CA408633447

Gene: SNTA1

Linked Data

• dbSNP Id: rs1600864236
• MyVariant Identifiers: chr20:g.32026721T>C (hg19) ; chr20:g.33438915T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438915T>C , CM000682.2:g.33438915T>C	GRCh38
NC_000020.10:g.32026721T>C , CM000682.1:g.32026721T>C	GRCh37
NC_000020.9:g.31490382T>C	NCBI36
NG_011622.1:g.9978A>G , LRG_332:g.9978A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.422A>G MANE Select	ENSP00000217381.2:p.Glu141Gly
ENST00000217381.2:c.422A>G	ENSP00000217381.2:p.Glu141Gly
NM_003098.2:c.422A>G , LRG_332t1:c.422A>G	NP_003089.1:p.Glu141Gly
XM_005260517.1:c.422A>G	XP_005260574.1:p.Glu141Gly
XM_011529007.1:c.422A>G	XP_011527309.1:p.Glu141Gly
XM_011529008.1:c.422A>G	XP_011527310.1:p.Glu141Gly
XR_936612.1:n.655A>G
XM_024451971.1:c.95A>G	XP_024307739.1:p.Glu32Gly
NM_003098.3:c.422A>G MANE Select	NP_003089.1:p.Glu141Gly