Canonical Allele Identifier: CA2059285064
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501478A= , CM000674.2:g.102501478A= GRCh38
NC_000012.11:g.102895256A= , CM000674.1:g.102895256A= GRCh37
NC_000012.10:g.101419386A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17590A=