Canonical Allele Identifier: CA1704517799
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46033005A= , CM000669.2:g.46033005A= GRCh38
NC_000007.13:g.46072603A= , CM000669.1:g.46072603A= GRCh37
NC_000007.12:g.46039128A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745203.1:n.1270-3613A=