Canonical Allele Identifier: CA1206156997
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586593G= , CM000663.2:g.169586593G= GRCh38
NC_000001.10:g.169555831G= , CM000663.1:g.169555831G= GRCh37
NC_000001.9:g.167822455G= NCBI36
NG_011806.1:g.4939C= , LRG_553:g.4939C=

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-526C= XP_016856149.1:n.-526C=