Canonical Allele Identifier: CA2258509552
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.37666305T>G , CM000679.2:g.37666305T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
XR_002958135.1:n.243-17866T>G