Canonical Allele Identifier: CA2185570152
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.69755669T= , CM000677.2:g.69755669T= GRCh38
NC_000015.9:g.70048008T= , CM000677.1:g.70048008T= GRCh37
NC_000015.8:g.67835062T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001751592.2:n.86-487T=