Canonical Allele Identifier: CA1573933672
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660947G= , CM000667.2:g.113660947G= GRCh38
NC_000005.9:g.112996644G= , CM000667.1:g.112996644G= GRCh37
NC_000005.8:g.113024543G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27583G=