Canonical Allele Identifier: CA2809771339
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211630T>C , CM000679.2:g.50211630T>C GRCh38
NC_000017.10:g.48288991T>C , CM000679.1:g.48288991T>C GRCh37
NC_000017.9:g.45643990T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-2205T>C