Canonical Allele Identifier: CA2360753147

Gene: SNTA1

Linked Data

• dbSNP Id: rs746905146
• gnomAD v4: 20-33439062-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33439062G>A , CM000682.2:g.33439062G>A	GRCh38
NC_000020.10:g.32026868G>A , CM000682.1:g.32026868G>A	GRCh37
NC_000020.9:g.31490529G>A	NCBI36
NG_011622.1:g.9831C>T , LRG_332:g.9831C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.311-36C>T MANE Select	ENSP00000217381.2:n.311-36C>T
ENST00000217381.2:c.311-36C>T	ENSP00000217381.2:n.311-36C>T
NM_003098.2:c.311-36C>T , LRG_332t1:c.311-36C>T	NP_003089.1:n.311-36C>T
XM_005260517.1:c.311-36C>T	XP_005260574.1:n.311-36C>T
XM_011529007.1:c.311-36C>T	XP_011527309.1:n.311-36C>T
XM_011529008.1:c.311-36C>T	XP_011527310.1:n.311-36C>T
XR_936612.1:n.544-36C>T
XM_024451971.1:c.-17-36C>T	XP_024307739.1:n.-17-36C>T
NM_003098.3:c.311-36C>T MANE Select	NP_003089.1:n.311-36C>T