Canonical Allele Identifier: CA518861149

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548370A>G , CM000685.2:g.139548370A>G	GRCh38
NC_000023.10:g.138630529A>G , CM000685.1:g.138630529A>G	GRCh37
NC_000023.9:g.138458195A>G	NCBI36
NG_007994.1:g.22635A>G , LRG_556:g.22635A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.399A>G MANE Select	ENSP00000218099.2:p.Thr133=
ENST00000643157.1:n.1066A>G
ENST00000218099.6:c.399A>G	ENSP00000218099.2:p.Thr133=
ENST00000394090.2:c.285A>G	ENSP00000377650.2:p.Thr95=
ENST00000479617.2:n.352A>G
NM_000133.3:c.399A>G , LRG_556t1:c.399A>G	NP_000124.1:p.Thr133=
NM_001313913.1:c.285A>G	NP_001300842.1:p.Thr95=
XM_005262397.3:c.392-2692A>G	XP_005262454.1:n.392-2692A>G
XM_005262397.4:c.392-2692A>G	XP_005262454.1:n.392-2692A>G
NM_000133.4:c.399A>G MANE Select	NP_000124.1:p.Thr133=
NM_001313913.2:c.285A>G	NP_001300842.1:p.Thr95=