Canonical Allele Identifier: CA414439424

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548480G>A , CM000685.2:g.139548480G>A	GRCh38
NC_000023.10:g.138630639G>A , CM000685.1:g.138630639G>A	GRCh37
NC_000023.9:g.138458305G>A	NCBI36
NG_007994.1:g.22745G>A , LRG_556:g.22745G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.509G>A MANE Select	ENSP00000218099.2:p.Cys170Tyr
ENST00000643157.1:n.1176G>A
ENST00000218099.6:c.509G>A	ENSP00000218099.2:p.Cys170Tyr
ENST00000394090.2:c.395G>A	ENSP00000377650.2:p.Cys132Tyr
NM_000133.3:c.509G>A , LRG_556t1:c.509G>A	NP_000124.1:p.Cys170Tyr
NM_001313913.1:c.395G>A	NP_001300842.1:p.Cys132Tyr
XM_005262397.3:c.392-2582G>A	XP_005262454.1:n.392-2582G>A
XM_005262397.4:c.392-2582G>A	XP_005262454.1:n.392-2582G>A
NM_000133.4:c.509G>A MANE Select	NP_000124.1:p.Cys170Tyr
NM_001313913.2:c.395G>A	NP_001300842.1:p.Cys132Tyr