Canonical Allele Identifier: CA1206156947
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586496G= , CM000663.2:g.169586496G= GRCh38
NC_000001.10:g.169555734G= , CM000663.1:g.169555734G= GRCh37
NC_000001.9:g.167822358G= NCBI36
NG_011806.1:g.5036C= , LRG_553:g.5036C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-110C= ENSP00000356770.3:n.-110C=
ENST00000367797.7:c.-110C= ENSP00000356771.3:n.-110C=
NM_000130.4:c.-110C= , LRG_553t1:c.-110C= NP_000121.2:n.-110C=
XM_017000660.2:c.-429C= XP_016856149.1:n.-429C=