Canonical Allele Identifier: CA408634688

Gene: SNTA1

Linked Data

• dbSNP Id: rs2146815249
• gnomAD v4: 20-33443565-G-A
• MyVariant Identifiers: chr20:g.32031371G>A (hg19) ; chr20:g.33443565G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443565G>A , CM000682.2:g.33443565G>A	GRCh38
NC_000020.10:g.32031371G>A , CM000682.1:g.32031371G>A	GRCh37
NC_000020.9:g.31495032G>A	NCBI36
NG_011622.1:g.5328C>T , LRG_332:g.5328C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.56C>T MANE Select	ENSP00000217381.2:p.Ala19Val
ENST00000217381.2:c.56C>T	ENSP00000217381.2:p.Ala19Val
NM_003098.2:c.56C>T , LRG_332t1:c.56C>T	NP_003089.1:p.Ala19Val
XM_005260517.1:c.56C>T	XP_005260574.1:p.Ala19Val
XM_011529007.1:c.56C>T	XP_011527309.1:p.Ala19Val
XM_011529008.1:c.56C>T	XP_011527310.1:p.Ala19Val
XR_936612.1:n.289C>T
NM_003098.3:c.56C>T MANE Select	NP_003089.1:p.Ala19Val