Canonical Allele Identifier: CA518861179

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138630547C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548388C>A , CM000685.2:g.139548388C>A	GRCh38
NC_000023.10:g.138630547C>A , CM000685.1:g.138630547C>A	GRCh37
NC_000023.9:g.138458213C>A	NCBI36
NG_007994.1:g.22653C>A , LRG_556:g.22653C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.417C>A MANE Select	ENSP00000218099.2:p.Gly139=
ENST00000643157.1:n.1084C>A
ENST00000218099.6:c.417C>A	ENSP00000218099.2:p.Gly139=
ENST00000394090.2:c.303C>A	ENSP00000377650.2:p.Gly101=
ENST00000479617.2:n.370C>A
NM_000133.3:c.417C>A , LRG_556t1:c.417C>A	NP_000124.1:p.Gly139=
NM_001313913.1:c.303C>A	NP_001300842.1:p.Gly101=
XM_005262397.3:c.392-2674C>A	XP_005262454.1:n.392-2674C>A
XM_005262397.4:c.392-2674C>A	XP_005262454.1:n.392-2674C>A
NM_000133.4:c.417C>A MANE Select	NP_000124.1:p.Gly139=
NM_001313913.2:c.303C>A	NP_001300842.1:p.Gly101=