Canonical Allele Identifier: CA2715004072
Gene:

Linked Data

dbSNP Id: rs1004310968

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87913807C>A , CM000669.2:g.87913807C>A GRCh38
NC_000007.13:g.87543122C>A , CM000669.1:g.87543122C>A GRCh37
NC_000007.12:g.87381058C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927723.1:n.148+94G>T
XR_927724.1:n.192+94G>T