Canonical Allele Identifier: CA414439016
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139548416G>A , CM000685.2:g.139548416G>A GRCh38
NC_000023.10:g.138630575G>A , CM000685.1:g.138630575G>A GRCh37
NC_000023.9:g.138458241G>A NCBI36
NG_007994.1:g.22681G>A , LRG_556:g.22681G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.445G>A MANE Select ENSP00000218099.2:p.Ala149Thr
ENST00000643157.1:n.1112G>A
ENST00000218099.6:c.445G>A ENSP00000218099.2:p.Ala149Thr
ENST00000394090.2:c.331G>A ENSP00000377650.2:p.Ala111Thr
NM_000133.3:c.445G>A , LRG_556t1:c.445G>A NP_000124.1:p.Ala149Thr
NM_001313913.1:c.331G>A NP_001300842.1:p.Ala111Thr
XM_005262397.3:c.392-2646G>A XP_005262454.1:n.392-2646G>A
XM_005262397.4:c.392-2646G>A XP_005262454.1:n.392-2646G>A
NM_000133.4:c.445G>A MANE Select NP_000124.1:p.Ala149Thr
NM_001313913.2:c.331G>A NP_001300842.1:p.Ala111Thr