Canonical Allele Identifier: CA1950112379
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6318921C= , CM000673.2:g.6318921C= GRCh38
NC_000011.9:g.6340151C= , CM000673.1:g.6340151C= GRCh37
NC_000011.8:g.6296727C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930997.1:n.720+701C=