Canonical Allele Identifier: CA2360753008

Gene: SNTA1

Linked Data

• dbSNP Id: rs1481686349
• gnomAD v4: 20-33438693-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438693C>A , CM000682.2:g.33438693C>A	GRCh38
NC_000020.10:g.32026499C>A , CM000682.1:g.32026499C>A	GRCh37
NC_000020.9:g.31490160C>A	NCBI36
NG_011622.1:g.10200G>T , LRG_332:g.10200G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+148G>T MANE Select	ENSP00000217381.2:n.496+148G>T
ENST00000217381.2:c.496+148G>T	ENSP00000217381.2:n.496+148G>T
NM_003098.2:c.496+148G>T , LRG_332t1:c.496+148G>T	NP_003089.1:n.496+148G>T
XM_005260517.1:c.496+148G>T	XP_005260574.1:n.496+148G>T
XM_011529007.1:c.496+148G>T	XP_011527309.1:n.496+148G>T
XM_011529008.1:c.496+148G>T	XP_011527310.1:n.496+148G>T
XR_936612.1:n.729+148G>T
XM_024451971.1:c.169+148G>T	XP_024307739.1:n.169+148G>T
NM_003098.3:c.496+148G>T MANE Select	NP_003089.1:n.496+148G>T