Canonical Allele Identifier: CA1649475267
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98048098T= , CM000668.2:g.98048098T= GRCh38
NC_000006.11:g.98495974T= , CM000668.1:g.98495974T= GRCh37
NC_000006.10:g.98602695T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.372-51088T=
XR_942809.1:n.372-51088T=