Canonical Allele Identifier: CA1816697742
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.123753552T= , CM000670.2:g.123753552T= GRCh38
NC_000008.10:g.124765792T= , CM000670.1:g.124765792T= GRCh37
NC_000008.9:g.124834973T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928607.1:n.153-11231T=
XR_928607.3:n.324-11231T=