Canonical Allele Identifier: CA2538205488
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601446G>C , CM000666.2:g.134601446G>C GRCh38
NC_000004.11:g.135522601G>C , CM000666.1:g.135522601G>C GRCh37
NC_000004.10:g.135742051G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939212.1:n.410+14087G>C
XR_939214.1:n.392+14087G>C
XR_939214.2:n.392+14087G>C