Canonical Allele Identifier: CA414438783

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138630527A>T (hg19) ; chrX:g.139548368A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548368A>T , CM000685.2:g.139548368A>T	GRCh38
NC_000023.10:g.138630527A>T , CM000685.1:g.138630527A>T	GRCh37
NC_000023.9:g.138458193A>T	NCBI36
NG_007994.1:g.22633A>T , LRG_556:g.22633A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.397A>T MANE Select	ENSP00000218099.2:p.Thr133Ser
ENST00000643157.1:n.1064A>T
ENST00000218099.6:c.397A>T	ENSP00000218099.2:p.Thr133Ser
ENST00000394090.2:c.283A>T	ENSP00000377650.2:p.Thr95Ser
ENST00000479617.2:n.350A>T
NM_000133.3:c.397A>T , LRG_556t1:c.397A>T	NP_000124.1:p.Thr133Ser
NM_001313913.1:c.283A>T	NP_001300842.1:p.Thr95Ser
XM_005262397.3:c.392-2694A>T	XP_005262454.1:n.392-2694A>T
XM_005262397.4:c.392-2694A>T	XP_005262454.1:n.392-2694A>T
NM_000133.4:c.397A>T MANE Select	NP_000124.1:p.Thr133Ser
NM_001313913.2:c.283A>T	NP_001300842.1:p.Thr95Ser