Canonical Allele Identifier: CA2022606229
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.24617866T= , CM000674.2:g.24617866T= GRCh38
NC_000012.11:g.24770800T= , CM000674.1:g.24770800T= GRCh37
NC_000012.10:g.24662067T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749046.1:n.425-56A=