Canonical Allele Identifier: CA1206148914

Gene: F5

Linked Data

• dbSNP Id: rs9332524

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572602G>C , CM000663.2:g.169572602G>C	GRCh38
NC_000001.10:g.169541840G>C , CM000663.1:g.169541840G>C	GRCh37
NC_000001.9:g.167808464G>C	NCBI36
NG_011806.1:g.18930C>G , LRG_553:g.18930C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.251-259C>G MANE Select	ENSP00000356771.3:n.251-259C>G
ENST00000367796.3:c.251-259C>G	ENSP00000356770.3:n.251-259C>G
ENST00000367797.7:c.251-259C>G	ENSP00000356771.3:n.251-259C>G
NM_000130.4:c.251-259C>G , LRG_553t1:c.251-259C>G	NP_000121.2:n.251-259C>G
XM_017000660.2:c.-161-259C>G	XP_016856149.1:n.-161-259C>G
NM_000130.5:c.251-259C>G MANE Select	NP_000121.2:n.251-259C>G