Canonical Allele Identifier: CA2185570150
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.69755668G= , CM000677.2:g.69755668G= GRCh38
NC_000015.9:g.70048007G= , CM000677.1:g.70048007G= GRCh37
NC_000015.8:g.67835061G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001751592.2:n.86-488G=