Canonical Allele Identifier: CA1880834322
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576794C= , CM000671.2:g.129576794C= GRCh38
NC_000009.11:g.132339073C= , CM000671.1:g.132339073C= GRCh37
NC_000009.10:g.131378894C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1196C=