Canonical Allele Identifier: CA1573933689
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660995T= , CM000667.2:g.113660995T= GRCh38
NC_000005.9:g.112996692T= , CM000667.1:g.112996692T= GRCh37
NC_000005.8:g.113024591T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27631T=