Canonical Allele Identifier: CA1446423105
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.27743096C= , CM000666.2:g.27743096C= GRCh38
NC_000004.11:g.27744718C= , CM000666.1:g.27744718C= GRCh37
NC_000004.10:g.27353816C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925519.1:n.328-2325C=
XR_925519.2:n.401-2325C=