Canonical Allele Identifier: CA510252252

Gene: SNTA1

Linked Data

• dbSNP Id: rs1483766095
• gnomAD v2: 20-32026765-T-C
• gnomAD v4: 20-33438959-T-C
• MyVariant Identifiers: chr20:g.32026765T>C (hg19) ; chr20:g.33438959T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438959T>C , CM000682.2:g.33438959T>C	GRCh38
NC_000020.10:g.32026765T>C , CM000682.1:g.32026765T>C	GRCh37
NC_000020.9:g.31490426T>C	NCBI36
NG_011622.1:g.9934A>G , LRG_332:g.9934A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.378A>G MANE Select	ENSP00000217381.2:p.Thr126=
ENST00000217381.2:c.378A>G	ENSP00000217381.2:p.Thr126=
NM_003098.2:c.378A>G , LRG_332t1:c.378A>G	NP_003089.1:p.Thr126=
XM_005260517.1:c.378A>G	XP_005260574.1:p.Thr126=
XM_011529007.1:c.378A>G	XP_011527309.1:p.Thr126=
XM_011529008.1:c.378A>G	XP_011527310.1:p.Thr126=
XR_936612.1:n.611A>G
XM_024451971.1:c.51A>G	XP_024307739.1:p.Thr17=
NM_003098.3:c.378A>G MANE Select	NP_003089.1:p.Thr126=