Canonical Allele Identifier: CA872127444

Gene: F9

Linked Data

• dbSNP Id: rs1231984110
• MyVariant Identifiers: chrX:g.138643666A>T (hg19) ; chrX:g.139561507A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561507A>T , CM000685.2:g.139561507A>T	GRCh38
NC_000023.10:g.138643666A>T , CM000685.1:g.138643666A>T	GRCh37
NC_000023.9:g.138471332A>T	NCBI36
NG_007994.1:g.35772A>T , LRG_556:g.35772A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.839-17A>T MANE Select	ENSP00000218099.2:n.839-17A>T
ENST00000643157.1:n.1506-17A>T
ENST00000218099.6:c.839-17A>T	ENSP00000218099.2:n.839-17A>T
ENST00000394090.2:c.725-17A>T	ENSP00000377650.2:n.725-17A>T
NM_000133.3:c.839-17A>T , LRG_556t1:c.839-17A>T	NP_000124.1:n.839-17A>T
NM_001313913.1:c.725-17A>T	NP_001300842.1:n.725-17A>T
XM_005262397.3:c.710-17A>T	XP_005262454.1:n.710-17A>T
XM_005262397.4:c.710-17A>T	XP_005262454.1:n.710-17A>T
NM_000133.4:c.839-17A>T MANE Select	NP_000124.1:n.839-17A>T
NM_001313913.2:c.725-17A>T	NP_001300842.1:n.725-17A>T