Canonical Allele Identifier: CA414437950

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541180T>C , CM000685.2:g.139541180T>C	GRCh38
NC_000023.10:g.138623339T>C , CM000685.1:g.138623339T>C	GRCh37
NC_000023.9:g.138451005T>C	NCBI36
NG_007994.1:g.15445T>C , LRG_556:g.15445T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.382T>C MANE Select	ENSP00000218099.2:p.Cys128Arg
ENST00000218099.6:c.382T>C	ENSP00000218099.2:p.Cys128Arg
ENST00000394090.2:c.277+3794T>C	ENSP00000377650.2:n.277+3794T>C
ENST00000479617.2:n.335T>C
NM_000133.3:c.382T>C , LRG_556t1:c.382T>C	NP_000124.1:p.Cys128Arg
NM_001313913.1:c.277+3794T>C	NP_001300842.1:n.277+3794T>C
XM_005262397.3:c.382T>C	XP_005262454.1:p.Cys128Arg
XM_005262397.4:c.382T>C	XP_005262454.1:p.Cys128Arg
NM_000133.4:c.382T>C MANE Select	NP_000124.1:p.Cys128Arg
NM_001313913.2:c.277+3794T>C	NP_001300842.1:n.277+3794T>C