Canonical Allele Identifier: CA1519999009
Gene: F11-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186417096G= , CM000666.2:g.186417096G= GRCh38
NC_000004.11:g.187338250G= , CM000666.1:g.187338250G= GRCh37
NC_000004.10:g.187575244G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033900.1:n.214+83749C=
XR_427648.2:n.1186-760C=
XR_939587.1:n.1354-760C=
XR_939588.1:n.1074-760C=
NR_033901.2:n.1573-760C=