Canonical Allele Identifier: CA2059285003
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501355G= , CM000674.2:g.102501355G= GRCh38
NC_000012.11:g.102895133G= , CM000674.1:g.102895133G= GRCh37
NC_000012.10:g.101419263G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17467G=