Canonical Allele Identifier: CA10649609
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 338206
ClinVar RCV Id: RCV000285617 RCV000377650
dbSNP Id: rs41305789
gnomAD v2: 20-31995970-C-T
gnomAD v3: 20-33408164-C-T
gnomAD v4: 20-33408164-C-T
MyVariant Identifiers: chr20:g.31995970C>T (hg19) chr20:g.33408164C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33408164C>T , CM000682.2:g.33408164C>T GRCh38
NC_000020.10:g.31995970C>T , CM000682.1:g.31995970C>T GRCh37
NC_000020.9:g.31459631C>T NCBI36
NG_011622.1:g.40729G>A , LRG_332:g.40729G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.3:c.*343G>A MANE Select ENSP00000217381.2:n.*343G>A
ENST00000217381.2:c.*343G>A ENSP00000217381.2:n.*343G>A
NM_003098.2:c.*343G>A , LRG_332t1:c.*343G>A NP_003089.1:n.*343G>A
XM_005260517.1:c.*343G>A XP_005260574.1:n.*343G>A
XM_011529007.1:c.*402G>A XP_011527309.1:n.*402G>A
XM_011529008.1:c.*402G>A XP_011527310.1:n.*402G>A
XR_936612.1:n.1897G>A
XM_024451971.1:c.*343G>A XP_024307739.1:n.*343G>A
NM_003098.3:c.*343G>A MANE Select NP_003089.1:n.*343G>A
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