Canonical Allele Identifier: CA414443129

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138642918G>T (hg19) ; chrX:g.139560759G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560759G>T , CM000685.2:g.139560759G>T	GRCh38
NC_000023.10:g.138642918G>T , CM000685.1:g.138642918G>T	GRCh37
NC_000023.9:g.138470584G>T	NCBI36
NG_007994.1:g.35024G>T , LRG_556:g.35024G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.742G>T MANE Select	ENSP00000218099.2:p.Val248Phe
ENST00000643157.1:n.1409G>T
ENST00000218099.6:c.742G>T	ENSP00000218099.2:p.Val248Phe
ENST00000394090.2:c.628G>T	ENSP00000377650.2:p.Val210Phe
NM_000133.3:c.742G>T , LRG_556t1:c.742G>T	NP_000124.1:p.Val248Phe
NM_001313913.1:c.628G>T	NP_001300842.1:p.Val210Phe
XM_005262397.3:c.613G>T	XP_005262454.1:p.Val205Phe
XM_005262397.4:c.613G>T	XP_005262454.1:p.Val205Phe
NM_000133.4:c.742G>T MANE Select	NP_000124.1:p.Val248Phe
NM_001313913.2:c.628G>T	NP_001300842.1:p.Val210Phe