Canonical Allele Identifier: CA2638676352
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211907T>C , CM000679.2:g.50211907T>C GRCh38
NC_000017.10:g.48289268T>C , CM000679.1:g.48289268T>C GRCh37
NC_000017.9:g.45644267T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-1928T>C