Canonical Allele Identifier: CA518861353

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138630622A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548463A>T , CM000685.2:g.139548463A>T	GRCh38
NC_000023.10:g.138630622A>T , CM000685.1:g.138630622A>T	GRCh37
NC_000023.9:g.138458288A>T	NCBI36
NG_007994.1:g.22728A>T , LRG_556:g.22728A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.492A>T MANE Select	ENSP00000218099.2:p.Ala164=
ENST00000643157.1:n.1159A>T
ENST00000218099.6:c.492A>T	ENSP00000218099.2:p.Ala164=
ENST00000394090.2:c.378A>T	ENSP00000377650.2:p.Ala126=
NM_000133.3:c.492A>T , LRG_556t1:c.492A>T	NP_000124.1:p.Ala164=
NM_001313913.1:c.378A>T	NP_001300842.1:p.Ala126=
XM_005262397.3:c.392-2599A>T	XP_005262454.1:n.392-2599A>T
XM_005262397.4:c.392-2599A>T	XP_005262454.1:n.392-2599A>T
NM_000133.4:c.492A>T MANE Select	NP_000124.1:p.Ala164=
NM_001313913.2:c.378A>T	NP_001300842.1:p.Ala126=