Canonical Allele Identifier: CA2059284976
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501318C= , CM000674.2:g.102501318C= GRCh38
NC_000012.11:g.102895096C= , CM000674.1:g.102895096C= GRCh37
NC_000012.10:g.101419226C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749289.1:n.1952+17430C=