Canonical Allele Identifier: CA1140164166
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586581C= , CM000663.2:g.169586581C= GRCh38
NC_000001.10:g.169555819C= , CM000663.1:g.169555819C= GRCh37
NC_000001.9:g.167822443C= NCBI36
NG_011806.1:g.4951G= , LRG_553:g.4951G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-195G= ENSP00000356770.3:n.-195G=
ENST00000367797.7:c.-195G= ENSP00000356771.3:n.-195G=
XM_017000660.2:c.-514G= XP_016856149.1:n.-514G=