Canonical Allele Identifier: CA2059285006
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501366G= , CM000674.2:g.102501366G= GRCh38
NC_000012.11:g.102895144G= , CM000674.1:g.102895144G= GRCh37
NC_000012.10:g.101419274G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17478G=