Canonical Allele Identifier: CA635719739

Gene: SNTA1

Linked Data

• dbSNP Id: rs1245409205
• gnomAD v2: 20-32026616-C-A
• gnomAD v4: 20-33438810-C-A
• MyVariant Identifiers: chr20:g.32026616C>A (hg19) ; chr20:g.33438810C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438810C>A , CM000682.2:g.33438810C>A	GRCh38
NC_000020.10:g.32026616C>A , CM000682.1:g.32026616C>A	GRCh37
NC_000020.9:g.31490277C>A	NCBI36
NG_011622.1:g.10083G>T , LRG_332:g.10083G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+31G>T MANE Select	ENSP00000217381.2:n.496+31G>T
ENST00000217381.2:c.496+31G>T	ENSP00000217381.2:n.496+31G>T
NM_003098.2:c.496+31G>T , LRG_332t1:c.496+31G>T	NP_003089.1:n.496+31G>T
XM_005260517.1:c.496+31G>T	XP_005260574.1:n.496+31G>T
XM_011529007.1:c.496+31G>T	XP_011527309.1:n.496+31G>T
XM_011529008.1:c.496+31G>T	XP_011527310.1:n.496+31G>T
XR_936612.1:n.729+31G>T
XM_024451971.1:c.169+31G>T	XP_024307739.1:n.169+31G>T
NM_003098.3:c.496+31G>T MANE Select	NP_003089.1:n.496+31G>T