Canonical Allele Identifier: CA2142026600
Community Standard Title: NC_000014.9:g.63133372T=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.63133372T= , CM000676.2:g.63133372T= GRCh38
NC_000014.8:g.63600090T= , CM000676.1:g.63600090T= GRCh37
NC_000014.7:g.62669843T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943934.1:n.730-5161A=
XR_943934.3:n.675-5161A=
XR_943935.1:n.467-5161A=
XR_943935.3:n.773-5161A=
XR_943936.1:n.623-5161A=
XR_943936.3:n.938-5161A=
XR_943938.1:n.173-5161A=
XR_943938.3:n.649-5161A=