Canonical Allele Identifier: CA1519999022
Gene: F11-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186417121C= , CM000666.2:g.186417121C= GRCh38
NC_000004.11:g.187338275C= , CM000666.1:g.187338275C= GRCh37
NC_000004.10:g.187575269C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033900.1:n.214+83724G=
XR_427648.2:n.1186-785G=
XR_939587.1:n.1354-785G=
XR_939588.1:n.1074-785G=
NR_033901.2:n.1573-785G=