Canonical Allele Identifier: CA1760507853
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907547G= , CM000670.2:g.5907547G= GRCh38
NC_000008.10:g.5765069G= , CM000670.1:g.5765069G= GRCh37
NC_000008.9:g.5752477G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-7816C=
XR_941375.1:n.308-7816C=
XR_941376.1:n.406-7816C=
XR_941377.1:n.308-7816C=
XR_941378.1:n.216-7816C=
XR_001745765.1:n.308-7816C=
XR_001745766.1:n.406-7816C=
XR_001745767.1:n.216-7816C=
XR_001745768.1:n.308-7816C=
XR_941374.2:n.308-7816C=
XR_941375.2:n.308-7816C=