Canonical Allele Identifier: CA2185570202
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.69755777A= , CM000677.2:g.69755777A= GRCh38
NC_000015.9:g.70048116A= , CM000677.1:g.70048116A= GRCh37
NC_000015.8:g.67835170A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001751592.2:n.86-379A=