Canonical Allele Identifier: CA589717573
Gene:

Linked Data

dbSNP Id: rs1192537829
gnomAD v2: 9-110855327-G-T
gnomAD v3: 9-108093046-G-T
gnomAD v4: 9-108093046-G-T
MyVariant Identifiers: chr9:g.110855327G>T (hg19) chr9:g.108093046G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108093046G>T , CM000671.2:g.108093046G>T GRCh38
NC_000009.11:g.110855327G>T , CM000671.1:g.110855327G>T GRCh37
NC_000009.10:g.109895148G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930239.1:n.461-39752C>A
XR_001746881.1:n.668-39752C>A
XR_001746882.1:n.668-39752C>A
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