Canonical Allele Identifier: CA1573933664
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660938G= , CM000667.2:g.113660938G= GRCh38
NC_000005.9:g.112996635G= , CM000667.1:g.112996635G= GRCh37
NC_000005.8:g.113024534G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27574G=