Canonical Allele Identifier: CA1206156994
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586586C= , CM000663.2:g.169586586C= GRCh38
NC_000001.10:g.169555824C= , CM000663.1:g.169555824C= GRCh37
NC_000001.9:g.167822448C= NCBI36
NG_011806.1:g.4946G= , LRG_553:g.4946G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-200G= ENSP00000356770.3:n.-200G=
ENST00000367797.7:c.-200G= ENSP00000356771.3:n.-200G=
XM_017000660.2:c.-519G= XP_016856149.1:n.-519G=