Canonical Allele Identifier: CA2360752963

Gene: SNTA1

Linked Data

• dbSNP Id: rs1990499658

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438598G>A , CM000682.2:g.33438598G>A	GRCh38
NC_000020.10:g.32026404G>A , CM000682.1:g.32026404G>A	GRCh37
NC_000020.9:g.31490065G>A	NCBI36
NG_011622.1:g.10295C>T , LRG_332:g.10295C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+243C>T MANE Select	ENSP00000217381.2:n.496+243C>T
ENST00000217381.2:c.496+243C>T	ENSP00000217381.2:n.496+243C>T
NM_003098.2:c.496+243C>T , LRG_332t1:c.496+243C>T	NP_003089.1:n.496+243C>T
XM_005260517.1:c.496+243C>T	XP_005260574.1:n.496+243C>T
XM_011529007.1:c.496+243C>T	XP_011527309.1:n.496+243C>T
XM_011529008.1:c.496+243C>T	XP_011527310.1:n.496+243C>T
XR_936612.1:n.729+243C>T
XM_024451971.1:c.169+243C>T	XP_024307739.1:n.169+243C>T
NM_003098.3:c.496+243C>T MANE Select	NP_003089.1:n.496+243C>T