Canonical Allele Identifier: CA1796404086
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.79191166C= , CM000670.2:g.79191166C= GRCh38
NC_000008.10:g.80103401C= , CM000670.1:g.80103401C= GRCh37
NC_000008.9:g.80265956C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745720.1:n.105+795C=