Canonical Allele Identifier: CA2059285062
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501477C= , CM000674.2:g.102501477C= GRCh38
NC_000012.11:g.102895255C= , CM000674.1:g.102895255C= GRCh37
NC_000012.10:g.101419385C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749289.1:n.1952+17589C=