Canonical Allele Identifier: CA1817441666
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125478327A= , CM000670.2:g.125478327A= GRCh38
NC_000008.10:g.126490569A= , CM000670.1:g.126490569A= GRCh37
NC_000008.9:g.126559751A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+5013A=