Canonical Allele Identifier: CA3134681058
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98048076A>C , CM000668.2:g.98048076A>C GRCh38
NC_000006.11:g.98495952A>C , CM000668.1:g.98495952A>C GRCh37
NC_000006.10:g.98602673A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.372-51110A>C
XR_942809.1:n.372-51110A>C