Canonical Allele Identifier: CA1017041461

Gene: SNTA1

Linked Data

• dbSNP Id: rs1990500505
• gnomAD v3: 20-33438624-A-G
• gnomAD v4: 20-33438624-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438624A>G , CM000682.2:g.33438624A>G	GRCh38
NC_000020.10:g.32026430A>G , CM000682.1:g.32026430A>G	GRCh37
NC_000020.9:g.31490091A>G	NCBI36
NG_011622.1:g.10269T>C , LRG_332:g.10269T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+217T>C MANE Select	ENSP00000217381.2:n.496+217T>C
ENST00000217381.2:c.496+217T>C	ENSP00000217381.2:n.496+217T>C
NM_003098.2:c.496+217T>C , LRG_332t1:c.496+217T>C	NP_003089.1:n.496+217T>C
XM_005260517.1:c.496+217T>C	XP_005260574.1:n.496+217T>C
XM_011529007.1:c.496+217T>C	XP_011527309.1:n.496+217T>C
XM_011529008.1:c.496+217T>C	XP_011527310.1:n.496+217T>C
XR_936612.1:n.729+217T>C
XM_024451971.1:c.169+217T>C	XP_024307739.1:n.169+217T>C
NM_003098.3:c.496+217T>C MANE Select	NP_003089.1:n.496+217T>C