Canonical Allele Identifier: CA1691656499
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957959A= , CM000669.2:g.17957959A= GRCh38
NC_000007.13:g.17997582A= , CM000669.1:g.17997582A= GRCh37
NC_000007.12:g.17964107A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-711A=