Canonical Allele Identifier: CA518862945

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138642914T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560755T>G , CM000685.2:g.139560755T>G	GRCh38
NC_000023.10:g.138642914T>G , CM000685.1:g.138642914T>G	GRCh37
NC_000023.9:g.138470580T>G	NCBI36
NG_007994.1:g.35020T>G , LRG_556:g.35020T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.738T>G MANE Select	ENSP00000218099.2:p.Gly246=
ENST00000643157.1:n.1405T>G
ENST00000218099.6:c.738T>G	ENSP00000218099.2:p.Gly246=
ENST00000394090.2:c.624T>G	ENSP00000377650.2:p.Gly208=
NM_000133.3:c.738T>G , LRG_556t1:c.738T>G	NP_000124.1:p.Gly246=
NM_001313913.1:c.624T>G	NP_001300842.1:p.Gly208=
XM_005262397.3:c.609T>G	XP_005262454.1:p.Gly203=
XM_005262397.4:c.609T>G	XP_005262454.1:p.Gly203=
NM_000133.4:c.738T>G MANE Select	NP_000124.1:p.Gly246=
NM_001313913.2:c.624T>G	NP_001300842.1:p.Gly208=