Canonical Allele Identifier: CA1439212980
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578359G= , CM000666.2:g.12578359G= GRCh38
NC_000004.11:g.12579983G= , CM000666.1:g.12579983G= GRCh37
NC_000004.10:g.12189081G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+30983C=
XR_001741374.1:n.254+44296C=
XR_925406.3:n.140+30983C=