Canonical Allele Identifier: CA414443734

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138643014G>T (hg19) ; chrX:g.139560855G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560855G>T , CM000685.2:g.139560855G>T	GRCh38
NC_000023.10:g.138643014G>T , CM000685.1:g.138643014G>T	GRCh37
NC_000023.9:g.138470680G>T	NCBI36
NG_007994.1:g.35120G>T , LRG_556:g.35120G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.838G>T MANE Select	ENSP00000218099.2:p.Gly280Cys
ENST00000643157.1:n.1505G>T
ENST00000218099.6:c.838G>T	ENSP00000218099.2:p.Gly280Cys
ENST00000394090.2:c.724G>T	ENSP00000377650.2:p.Gly242Cys
NM_000133.3:c.838G>T , LRG_556t1:c.838G>T	NP_000124.1:p.Gly280Cys
NM_001313913.1:c.724G>T	NP_001300842.1:p.Gly242Cys
XM_005262397.3:c.709G>T	XP_005262454.1:p.Gly237Cys
XM_005262397.4:c.709G>T	XP_005262454.1:p.Gly237Cys
NM_000133.4:c.838G>T MANE Select	NP_000124.1:p.Gly280Cys
NM_001313913.2:c.724G>T	NP_001300842.1:p.Gly242Cys