Canonical Allele Identifier: CA1017044186

Gene: SNTA1

Linked Data

• dbSNP Id: rs1376407988
• gnomAD v3: 20-33443714-C-A
• gnomAD v4: 20-33443714-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443714C>A , CM000682.2:g.33443714C>A	GRCh38
NC_000020.10:g.32031520C>A , CM000682.1:g.32031520C>A	GRCh37
NC_000020.9:g.31495181C>A	NCBI36
NG_011622.1:g.5179G>T , LRG_332:g.5179G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000217381.3:c.-94G>T MANE Select	ENSP00000217381.2:n.-94G>T
ENST00000217381.2:c.-94G>T	ENSP00000217381.2:n.-94G>T
NM_003098.2:c.-94G>T , LRG_332t1:c.-94G>T	NP_003089.1:n.-94G>T
XM_005260517.1:c.-94G>T	XP_005260574.1:n.-94G>T
XM_011529007.1:c.-94G>T	XP_011527309.1:n.-94G>T
XM_011529008.1:c.-94G>T	XP_011527310.1:n.-94G>T
XR_936612.1:n.140G>T
NM_003098.3:c.-94G>T MANE Select	NP_003089.1:n.-94G>T