Canonical Allele Identifier: CA1206156952
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586503G= , CM000663.2:g.169586503G= GRCh38
NC_000001.10:g.169555741G= , CM000663.1:g.169555741G= GRCh37
NC_000001.9:g.167822365G= NCBI36
NG_011806.1:g.5029C= , LRG_553:g.5029C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-117C= ENSP00000356770.3:n.-117C=
ENST00000367797.7:c.-117C= ENSP00000356771.3:n.-117C=
NM_000130.4:c.-117C= , LRG_553t1:c.-117C= NP_000121.2:n.-117C=
XM_017000660.2:c.-436C= XP_016856149.1:n.-436C=