Canonical Allele Identifier: CA743726882

Gene: SNTA1

Linked Data

• dbSNP Id: rs1013778871
• MyVariant Identifiers: chr20:g.32026353G>A (hg19) ; chr20:g.33438547G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438547G>A , CM000682.2:g.33438547G>A	GRCh38
NC_000020.10:g.32026353G>A , CM000682.1:g.32026353G>A	GRCh37
NC_000020.9:g.31490014G>A	NCBI36
NG_011622.1:g.10346C>T , LRG_332:g.10346C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+294C>T MANE Select	ENSP00000217381.2:n.496+294C>T
ENST00000217381.2:c.496+294C>T	ENSP00000217381.2:n.496+294C>T
NM_003098.2:c.496+294C>T , LRG_332t1:c.496+294C>T	NP_003089.1:n.496+294C>T
XM_005260517.1:c.496+294C>T	XP_005260574.1:n.496+294C>T
XM_011529007.1:c.496+294C>T	XP_011527309.1:n.496+294C>T
XM_011529008.1:c.496+294C>T	XP_011527310.1:n.496+294C>T
XR_936612.1:n.729+294C>T
XM_024451971.1:c.169+294C>T	XP_024307739.1:n.169+294C>T
NM_003098.3:c.496+294C>T MANE Select	NP_003089.1:n.496+294C>T