Canonical Allele Identifier: CA1128124438
Gene:

Linked Data

dbSNP Id: rs2098067326

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.111236644A>G , CM000671.2:g.111236644A>G GRCh38
NC_000009.11:g.113998924A>G , CM000671.1:g.113998924A>G GRCh37
NC_000009.10:g.113038745A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930247.1:n.476+36169T>C
XR_930248.1:n.556+36169T>C
XR_930249.1:n.476+36169T>C
XR_001746893.1:n.476+36169T>C
XR_001746894.1:n.476+36169T>C
XR_930247.2:n.476+36169T>C