Canonical Allele Identifier: CA1723810357
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87913744A= , CM000669.2:g.87913744A= GRCh38
NC_000007.13:g.87543059A= , CM000669.1:g.87543059A= GRCh37
NC_000007.12:g.87380995A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927723.1:n.148+157T=
XR_927724.1:n.192+157T=