Canonical Allele Identifier: CA1573933669
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660945T= , CM000667.2:g.113660945T= GRCh38
NC_000005.9:g.112996642T= , CM000667.1:g.112996642T= GRCh37
NC_000005.8:g.113024541T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27581T=