Canonical Allele Identifier: CA414436111
Gene: F9 HGNC NCBI

Linked Data

dbSNP Id: rs137852225

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139537138G>T , CM000685.2:g.139537138G>T GRCh38
NC_000023.10:g.138619297G>T , CM000685.1:g.138619297G>T GRCh37
NC_000023.9:g.138446963G>T NCBI36
NG_007994.1:g.11403G>T , LRG_556:g.11403G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.217G>T MANE Select ENSP00000218099.2:p.Glu73Ter
ENST00000218099.6:c.217G>T ENSP00000218099.2:p.Glu73Ter
ENST00000394090.2:c.217G>T ENSP00000377650.2:p.Glu73Ter
ENST00000479617.2:n.224G>T
NM_000133.3:c.217G>T , LRG_556t1:c.217G>T NP_000124.1:p.Glu73Ter
NM_001313913.1:c.217G>T NP_001300842.1:p.Glu73Ter
XM_005262397.3:c.217G>T XP_005262454.1:p.Glu73Ter
XM_005262397.4:c.217G>T XP_005262454.1:p.Glu73Ter
NM_000133.4:c.217G>T MANE Select NP_000124.1:p.Glu73Ter
NM_001313913.2:c.217G>T NP_001300842.1:p.Glu73Ter