Canonical Allele Identifier: CA121125

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551121A>G , CM000685.2:g.139551121A>G	GRCh38
NC_000023.10:g.138633280A>G , CM000685.1:g.138633280A>G	GRCh37
NC_000023.9:g.138460946A>G	NCBI36
NG_007994.1:g.25386A>G , LRG_556:g.25386A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000133.4:c.580A>G MANE Select	NP_000124.1:p.Thr194Ala
ENST00000218099.7:c.580A>G MANE Select	ENSP00000218099.2:p.Thr194Ala
NM_000133.3:c.580A>G , LRG_556t1:c.580A>G	NP_000124.1:p.Thr194Ala
NM_001313913.1:c.466A>G	NP_001300842.1:p.Thr156Ala
NM_001313913.2:c.466A>G	NP_001300842.1:p.Thr156Ala
ENST00000218099.6:c.580A>G	ENSP00000218099.2:p.Thr194Ala
ENST00000394090.2:c.466A>G	ENSP00000377650.2:p.Thr156Ala
ENST00000643157.1:n.1247A>G
XM_005262397.3:c.451A>G	XP_005262454.1:p.Thr151Ala
XM_005262397.4:c.451A>G	XP_005262454.1:p.Thr151Ala