Canonical Allele Identifier: CA414437775

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138623315C>T (hg19) ; chrX:g.139541156C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541156C>T , CM000685.2:g.139541156C>T	GRCh38
NC_000023.10:g.138623315C>T , CM000685.1:g.138623315C>T	GRCh37
NC_000023.9:g.138450981C>T	NCBI36
NG_007994.1:g.15421C>T , LRG_556:g.15421C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.358C>T MANE Select	ENSP00000218099.2:p.Pro120Ser
ENST00000218099.6:c.358C>T	ENSP00000218099.2:p.Pro120Ser
ENST00000394090.2:c.277+3770C>T	ENSP00000377650.2:n.277+3770C>T
ENST00000479617.2:n.311C>T
NM_000133.3:c.358C>T , LRG_556t1:c.358C>T	NP_000124.1:p.Pro120Ser
NM_001313913.1:c.277+3770C>T	NP_001300842.1:n.277+3770C>T
XM_005262397.3:c.358C>T	XP_005262454.1:p.Pro120Ser
XM_005262397.4:c.358C>T	XP_005262454.1:p.Pro120Ser
NM_000133.4:c.358C>T MANE Select	NP_000124.1:p.Pro120Ser
NM_001313913.2:c.277+3770C>T	NP_001300842.1:n.277+3770C>T