Canonical Allele Identifier: CA1206157009
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586611A= , CM000663.2:g.169586611A= GRCh38
NC_000001.10:g.169555849A= , CM000663.1:g.169555849A= GRCh37
NC_000001.9:g.167822473A= NCBI36
NG_011806.1:g.4921T= , LRG_553:g.4921T=

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-544T= XP_016856149.1:n.-544T=