Canonical Allele Identifier: CA589717556
Gene:

Linked Data

dbSNP Id: rs1409710016
gnomAD v2: 9-110855085-C-A
gnomAD v3: 9-108092804-C-A
gnomAD v4: 9-108092804-C-A
MyVariant Identifiers: chr9:g.110855085C>A (hg19) chr9:g.108092804C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092804C>A , CM000671.2:g.108092804C>A GRCh38
NC_000009.11:g.110855085C>A , CM000671.1:g.110855085C>A GRCh37
NC_000009.10:g.109894906C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930239.1:n.461-39510G>T
XR_001746881.1:n.668-39510G>T
XR_001746882.1:n.668-39510G>T
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