Canonical Allele Identifier: CA1439212606
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12577992G= , CM000666.2:g.12577992G= GRCh38
NC_000004.11:g.12579616G= , CM000666.1:g.12579616G= GRCh37
NC_000004.10:g.12188714G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31350C=
XR_001741374.1:n.254+44663C=
XR_925406.3:n.140+31350C=