Canonical Allele Identifier: CA858377605
Gene:

Linked Data

dbSNP Id: rs1386111719
gnomAD v3: 9-108092801-C-T
gnomAD v4: 9-108092801-C-T
MyVariant Identifiers: chr9:g.110855082C>T (hg19) chr9:g.108092801C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092801C>T , CM000671.2:g.108092801C>T GRCh38
NC_000009.11:g.110855082C>T , CM000671.1:g.110855082C>T GRCh37
NC_000009.10:g.109894903C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930239.1:n.461-39507G>A
XR_001746881.1:n.668-39507G>A
XR_001746882.1:n.668-39507G>A
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