Canonical Allele Identifier: CA2185570201
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.69755774A= , CM000677.2:g.69755774A= GRCh38
NC_000015.9:g.70048113A= , CM000677.1:g.70048113A= GRCh37
NC_000015.8:g.67835167A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001751592.2:n.86-382A=