Canonical Allele Identifier: CA2059285007
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501373C= , CM000674.2:g.102501373C= GRCh38
NC_000012.11:g.102895151C= , CM000674.1:g.102895151C= GRCh37
NC_000012.10:g.101419281C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17485C=