Canonical Allele Identifier: CA125569086
Gene:

Linked Data

dbSNP Id: rs1056307932

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113661022T>G , CM000667.2:g.113661022T>G GRCh38
NC_000005.9:g.112996719T>G , CM000667.1:g.112996719T>G GRCh37
NC_000005.8:g.113024618T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27658T>G