Canonical Allele Identifier: CA1817442111
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125478872G= , CM000670.2:g.125478872G= GRCh38
NC_000008.10:g.126491114G= , CM000670.1:g.126491114G= GRCh37
NC_000008.9:g.126560296G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+5558G=