Canonical Allele Identifier: CA414446108

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561820C>G , CM000685.2:g.139561820C>G	GRCh38
NC_000023.10:g.138643979C>G , CM000685.1:g.138643979C>G	GRCh37
NC_000023.9:g.138471645C>G	NCBI36
NG_007994.1:g.36085C>G , LRG_556:g.36085C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000133.4:c.1135C>G MANE Select	NP_000124.1:p.Arg379Gly
ENST00000218099.7:c.1135C>G MANE Select	ENSP00000218099.2:p.Arg379Gly
NM_000133.3:c.1135C>G , LRG_556t1:c.1135C>G	NP_000124.1:p.Arg379Gly
NM_001313913.1:c.1021C>G	NP_001300842.1:p.Arg341Gly
NM_001313913.2:c.1021C>G	NP_001300842.1:p.Arg341Gly
ENST00000218099.6:c.1135C>G	ENSP00000218099.2:p.Arg379Gly
ENST00000394090.2:c.1021C>G	ENSP00000377650.2:p.Arg341Gly
ENST00000643157.1:n.1723+79C>G
XM_005262397.3:c.1006C>G	XP_005262454.1:p.Arg336Gly
XM_005262397.4:c.1006C>G	XP_005262454.1:p.Arg336Gly