Canonical Allele Identifier: CA2760462809
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578305G>T , CM000666.2:g.12578305G>T GRCh38
NC_000004.11:g.12579929G>T , CM000666.1:g.12579929G>T GRCh37
NC_000004.10:g.12189027G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31037C>A
XR_001741374.1:n.254+44350C>A
XR_925406.3:n.140+31037C>A