Canonical Allele Identifier: CA2018040119
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.105596960T>G , CM000675.2:g.105596960T>G GRCh38
NC_000013.10:g.106249309T>G , CM000675.1:g.106249309T>G GRCh37
NC_000013.9:g.105047310T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931698.1:n.632-23613A>C
XR_931699.2:n.629-23613A>C