Canonical Allele Identifier: CA518862130

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138633378G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551219G>C , CM000685.2:g.139551219G>C	GRCh38
NC_000023.10:g.138633378G>C , CM000685.1:g.138633378G>C	GRCh37
NC_000023.9:g.138461044G>C	NCBI36
NG_007994.1:g.25484G>C , LRG_556:g.25484G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.678G>C MANE Select	ENSP00000218099.2:p.Arg226=
ENST00000643157.1:n.1345G>C
ENST00000218099.6:c.678G>C	ENSP00000218099.2:p.Arg226=
ENST00000394090.2:c.564G>C	ENSP00000377650.2:p.Arg188=
NM_000133.3:c.678G>C , LRG_556t1:c.678G>C	NP_000124.1:p.Arg226=
NM_001313913.1:c.564G>C	NP_001300842.1:p.Arg188=
XM_005262397.3:c.549G>C	XP_005262454.1:p.Arg183=
XM_005262397.4:c.549G>C	XP_005262454.1:p.Arg183=
NM_000133.4:c.678G>C MANE Select	NP_000124.1:p.Arg226=
NM_001313913.2:c.564G>C	NP_001300842.1:p.Arg188=