Canonical Allele Identifier: CA197846292
Gene:

Linked Data

dbSNP Id: rs73499106

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092862C>T , CM000671.2:g.108092862C>T GRCh38
NC_000009.11:g.110855143C>T , CM000671.1:g.110855143C>T GRCh37
NC_000009.10:g.109894964C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930239.1:n.461-39568G>A
XR_001746881.1:n.668-39568G>A
XR_001746882.1:n.668-39568G>A