Canonical Allele Identifier: CA1206157003
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586601G= , CM000663.2:g.169586601G= GRCh38
NC_000001.10:g.169555839G= , CM000663.1:g.169555839G= GRCh37
NC_000001.9:g.167822463G= NCBI36
NG_011806.1:g.4931C= , LRG_553:g.4931C=

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-534C= XP_016856149.1:n.-534C=