Canonical Allele Identifier: CA2360752939

Gene: SNTA1

Linked Data

• dbSNP Id: rs1568762026

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438534G>T , CM000682.2:g.33438534G>T	GRCh38
NC_000020.10:g.32026340G>T , CM000682.1:g.32026340G>T	GRCh37
NC_000020.9:g.31490001G>T	NCBI36
NG_011622.1:g.10359C>A , LRG_332:g.10359C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+307C>A MANE Select	ENSP00000217381.2:n.496+307C>A
ENST00000217381.2:c.496+307C>A	ENSP00000217381.2:n.496+307C>A
NM_003098.2:c.496+307C>A , LRG_332t1:c.496+307C>A	NP_003089.1:n.496+307C>A
XM_005260517.1:c.496+307C>A	XP_005260574.1:n.496+307C>A
XM_011529007.1:c.496+307C>A	XP_011527309.1:n.496+307C>A
XM_011529008.1:c.496+307C>A	XP_011527310.1:n.496+307C>A
XR_936612.1:n.729+307C>A
XM_024451971.1:c.169+307C>A	XP_024307739.1:n.169+307C>A
NM_003098.3:c.496+307C>A MANE Select	NP_003089.1:n.496+307C>A