Canonical Allele Identifier: CA414438918

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548398C>T , CM000685.2:g.139548398C>T	GRCh38
NC_000023.10:g.138630557C>T , CM000685.1:g.138630557C>T	GRCh37
NC_000023.9:g.138458223C>T	NCBI36
NG_007994.1:g.22663C>T , LRG_556:g.22663C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.427C>T MANE Select	ENSP00000218099.2:p.Gln143Ter
ENST00000643157.1:n.1094C>T
ENST00000218099.6:c.427C>T	ENSP00000218099.2:p.Gln143Ter
ENST00000394090.2:c.313C>T	ENSP00000377650.2:p.Gln105Ter
NM_000133.3:c.427C>T , LRG_556t1:c.427C>T	NP_000124.1:p.Gln143Ter
NM_001313913.1:c.313C>T	NP_001300842.1:p.Gln105Ter
XM_005262397.3:c.392-2664C>T	XP_005262454.1:n.392-2664C>T
XM_005262397.4:c.392-2664C>T	XP_005262454.1:n.392-2664C>T
NM_000133.4:c.427C>T MANE Select	NP_000124.1:p.Gln143Ter
NM_001313913.2:c.313C>T	NP_001300842.1:p.Gln105Ter