Canonical Allele Identifier: CA635719641
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1184856429
gnomAD v2: 20-32031513-G-A
gnomAD v3: 20-33443707-G-A
gnomAD v4: 20-33443707-G-A
MyVariant Identifiers: chr20:g.32031513G>A (hg19) chr20:g.33443707G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443707G>A , CM000682.2:g.33443707G>A GRCh38
NC_000020.10:g.32031513G>A , CM000682.1:g.32031513G>A GRCh37
NC_000020.9:g.31495174G>A NCBI36
NG_011622.1:g.5186C>T , LRG_332:g.5186C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.-87C>T MANE Select ENSP00000217381.2:n.-87C>T
ENST00000217381.2:c.-87C>T ENSP00000217381.2:n.-87C>T
NM_003098.2:c.-87C>T , LRG_332t1:c.-87C>T NP_003089.1:n.-87C>T
XM_005260517.1:c.-87C>T XP_005260574.1:n.-87C>T
XM_011529007.1:c.-87C>T XP_011527309.1:n.-87C>T
XM_011529008.1:c.-87C>T XP_011527310.1:n.-87C>T
XR_936612.1:n.147C>T
NM_003098.3:c.-87C>T MANE Select NP_003089.1:n.-87C>T
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