Canonical Allele Identifier: CA1817442002
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125478714T= , CM000670.2:g.125478714T= GRCh38
NC_000008.10:g.126490956T= , CM000670.1:g.126490956T= GRCh37
NC_000008.9:g.126560138T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+5400T=