Canonical Allele Identifier: CA2360753141

Gene: SNTA1

Linked Data

• dbSNP Id: rs1990515759
• gnomAD v4: 20-33439049-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33439049C>T , CM000682.2:g.33439049C>T	GRCh38
NC_000020.10:g.32026855C>T , CM000682.1:g.32026855C>T	GRCh37
NC_000020.9:g.31490516C>T	NCBI36
NG_011622.1:g.9844G>A , LRG_332:g.9844G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.311-23G>A MANE Select	ENSP00000217381.2:n.311-23G>A
ENST00000217381.2:c.311-23G>A	ENSP00000217381.2:n.311-23G>A
NM_003098.2:c.311-23G>A , LRG_332t1:c.311-23G>A	NP_003089.1:n.311-23G>A
XM_005260517.1:c.311-23G>A	XP_005260574.1:n.311-23G>A
XM_011529007.1:c.311-23G>A	XP_011527309.1:n.311-23G>A
XM_011529008.1:c.311-23G>A	XP_011527310.1:n.311-23G>A
XR_936612.1:n.544-23G>A
XM_024451971.1:c.-17-23G>A	XP_024307739.1:n.-17-23G>A
NM_003098.3:c.311-23G>A MANE Select	NP_003089.1:n.311-23G>A