Canonical Allele Identifier: CA2573599875

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572597T>G , CM000663.2:g.169572597T>G	GRCh38
NC_000001.10:g.169541835T>G , CM000663.1:g.169541835T>G	GRCh37
NC_000001.9:g.167808459T>G	NCBI36
NG_011806.1:g.18935A>C , LRG_553:g.18935A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.251-254A>C MANE Select	ENSP00000356771.3:n.251-254A>C
ENST00000367796.3:c.251-254A>C	ENSP00000356770.3:n.251-254A>C
ENST00000367797.7:c.251-254A>C	ENSP00000356771.3:n.251-254A>C
NM_000130.4:c.251-254A>C , LRG_553t1:c.251-254A>C	NP_000121.2:n.251-254A>C
XM_017000660.2:c.-161-254A>C	XP_016856149.1:n.-161-254A>C
NM_000130.5:c.251-254A>C MANE Select	NP_000121.2:n.251-254A>C