Canonical Allele Identifier: CA2248820165
Community Standard Title: NC_000017.11:g.13830489C=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.13830489C= , CM000679.2:g.13830489C= GRCh38
NC_000017.10:g.13733806C= , CM000679.1:g.13733806C= GRCh37
NC_000017.9:g.13674531C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001752794.1:n.288-3892G=
XR_001752796.1:n.288-3892G=
XR_001752797.1:n.221-3892G=
XR_934240.1:n.118-3892G=
XR_934241.1:n.118-3892G=
XR_934242.1:n.187+49813G=