Canonical Allele Identifier: CA858377669
Gene:

Linked Data

dbSNP Id: rs1314050642
MyVariant Identifiers: chr9:g.110855218A>G (hg19) chr9:g.108092937A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092937A>G , CM000671.2:g.108092937A>G GRCh38
NC_000009.11:g.110855218A>G , CM000671.1:g.110855218A>G GRCh37
NC_000009.10:g.109895039A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930239.1:n.461-39643T>C
XR_001746881.1:n.668-39643T>C
XR_001746882.1:n.668-39643T>C
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