Canonical Allele Identifier: CA414437636

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541142A>G , CM000685.2:g.139541142A>G	GRCh38
NC_000023.10:g.138623301A>G , CM000685.1:g.138623301A>G	GRCh37
NC_000023.9:g.138450967A>G	NCBI36
NG_007994.1:g.15407A>G , LRG_556:g.15407A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.344A>G MANE Select	ENSP00000218099.2:p.Tyr115Cys
ENST00000218099.6:c.344A>G	ENSP00000218099.2:p.Tyr115Cys
ENST00000394090.2:c.277+3756A>G	ENSP00000377650.2:n.277+3756A>G
ENST00000479617.2:n.297A>G
NM_000133.3:c.344A>G , LRG_556t1:c.344A>G	NP_000124.1:p.Tyr115Cys
NM_001313913.1:c.277+3756A>G	NP_001300842.1:n.277+3756A>G
XM_005262397.3:c.344A>G	XP_005262454.1:p.Tyr115Cys
XM_005262397.4:c.344A>G	XP_005262454.1:p.Tyr115Cys
NM_000133.4:c.344A>G MANE Select	NP_000124.1:p.Tyr115Cys
NM_001313913.2:c.277+3756A>G	NP_001300842.1:n.277+3756A>G