Canonical Allele Identifier: CA2581314083
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211709C>T , CM000679.2:g.50211709C>T GRCh38
NC_000017.10:g.48289070C>T , CM000679.1:g.48289070C>T GRCh37
NC_000017.9:g.45644069C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934838.1:n.43-2126C>T