Canonical Allele Identifier: CA2059284961
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501284C= , CM000674.2:g.102501284C= GRCh38
NC_000012.11:g.102895062C= , CM000674.1:g.102895062C= GRCh37
NC_000012.10:g.101419192C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749289.1:n.1952+17396C=