Canonical Allele Identifier: CA313279314
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs6141397
gnomAD v4: 20-33443796-C-A
MyVariant Identifiers: chr20:g.32031602C>A (hg19) chr20:g.33443796C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443796C>A , CM000682.2:g.33443796C>A GRCh38
NC_000020.10:g.32031602C>A , CM000682.1:g.32031602C>A GRCh37
NC_000020.9:g.31495263C>A NCBI36
NG_011622.1:g.5097G>T , LRG_332:g.5097G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.2:c.-176G>T ENSP00000217381.2:n.-176G>T
NM_003098.2:c.-176G>T , LRG_332t1:c.-176G>T NP_003089.1:n.-176G>T
XM_005260517.1:c.-176G>T XP_005260574.1:n.-176G>T
XM_011529007.1:c.-176G>T XP_011527309.1:n.-176G>T
XM_011529008.1:c.-176G>T XP_011527310.1:n.-176G>T
XR_936612.1:n.58G>T
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