Canonical Allele Identifier: CA336132759

Gene: F9

Linked Data

• dbSNP Id: rs1054992012
• MyVariant Identifiers: chrX:g.138623219T>G (hg19) ; chrX:g.139541060T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541060T>G , CM000685.2:g.139541060T>G	GRCh38
NC_000023.10:g.138623219T>G , CM000685.1:g.138623219T>G	GRCh37
NC_000023.9:g.138450885T>G	NCBI36
NG_007994.1:g.15325T>G , LRG_556:g.15325T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.278-16T>G MANE Select	ENSP00000218099.2:n.278-16T>G
ENST00000218099.6:c.278-16T>G	ENSP00000218099.2:n.278-16T>G
ENST00000394090.2:c.277+3674T>G	ENSP00000377650.2:n.277+3674T>G
ENST00000479617.2:n.242-27T>G
NM_000133.3:c.278-16T>G , LRG_556t1:c.278-16T>G	NP_000124.1:n.278-16T>G
NM_001313913.1:c.277+3674T>G	NP_001300842.1:n.277+3674T>G
XM_005262397.3:c.278-16T>G	XP_005262454.1:n.278-16T>G
XM_005262397.4:c.278-16T>G	XP_005262454.1:n.278-16T>G
NM_000133.4:c.278-16T>G MANE Select	NP_000124.1:n.278-16T>G
NM_001313913.2:c.277+3674T>G	NP_001300842.1:n.277+3674T>G