Canonical Allele Identifier: CA2760462798
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578036C>T , CM000666.2:g.12578036C>T GRCh38
NC_000004.11:g.12579660C>T , CM000666.1:g.12579660C>T GRCh37
NC_000004.10:g.12188758C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31306G>A
XR_001741374.1:n.254+44619G>A
XR_925406.3:n.140+31306G>A