Canonical Allele Identifier: CA1573933698
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113661029T= , CM000667.2:g.113661029T= GRCh38
NC_000005.9:g.112996726T= , CM000667.1:g.112996726T= GRCh37
NC_000005.8:g.113024625T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27665T=