Canonical Allele Identifier: CA1872408650
Gene:

Linked Data

dbSNP Id: rs2098067329

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.111236649T>C , CM000671.2:g.111236649T>C GRCh38
NC_000009.11:g.113998929T>C , CM000671.1:g.113998929T>C GRCh37
NC_000009.10:g.113038750T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930247.1:n.476+36164A>G
XR_930248.1:n.556+36164A>G
XR_930249.1:n.476+36164A>G
XR_001746893.1:n.476+36164A>G
XR_001746894.1:n.476+36164A>G
XR_930247.2:n.476+36164A>G