Canonical Allele Identifier: CA1206156957
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586508G= , CM000663.2:g.169586508G= GRCh38
NC_000001.10:g.169555746G= , CM000663.1:g.169555746G= GRCh37
NC_000001.9:g.167822370G= NCBI36
NG_011806.1:g.5024C= , LRG_553:g.5024C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-122C= ENSP00000356770.3:n.-122C=
ENST00000367797.7:c.-122C= ENSP00000356771.3:n.-122C=
NM_000130.4:c.-122C= , LRG_553t1:c.-122C= NP_000121.2:n.-122C=
XM_017000660.2:c.-441C= XP_016856149.1:n.-441C=