Canonical Allele Identifier: CA2059284979
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501321T= , CM000674.2:g.102501321T= GRCh38
NC_000012.11:g.102895099T= , CM000674.1:g.102895099T= GRCh37
NC_000012.10:g.101419229T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749289.1:n.1952+17433T=