Canonical Allele Identifier: CA2378344953
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.15440893T= , CM000683.2:g.15440893T= GRCh38
NC_000021.8:g.16813212T= , CM000683.1:g.16813212T= GRCh37
NC_000021.7:g.15735083T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754965.2:n.468+3131A=
XR_001754970.2:n.468+3131A=
XR_001754971.2:n.468+3131A=
XR_937593.1:n.552+333A=