Canonical Allele Identifier: CA414446446
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561889G>A , CM000685.2:g.139561889G>A GRCh38
NC_000023.10:g.138644048G>A , CM000685.1:g.138644048G>A GRCh37
NC_000023.9:g.138471714G>A NCBI36
NG_007994.1:g.36154G>A , LRG_556:g.36154G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.1204G>A MANE Select ENSP00000218099.2:p.Gly402Arg
ENST00000643157.1:n.1723+148G>A
ENST00000218099.6:c.1204G>A ENSP00000218099.2:p.Gly402Arg
ENST00000394090.2:c.1090G>A ENSP00000377650.2:p.Gly364Arg
NM_000133.3:c.1204G>A , LRG_556t1:c.1204G>A NP_000124.1:p.Gly402Arg
NM_001313913.1:c.1090G>A NP_001300842.1:p.Gly364Arg
XM_005262397.3:c.1075G>A XP_005262454.1:p.Gly359Arg
XM_005262397.4:c.1075G>A XP_005262454.1:p.Gly359Arg
NM_000133.4:c.1204G>A MANE Select NP_000124.1:p.Gly402Arg
NM_001313913.2:c.1090G>A NP_001300842.1:p.Gly364Arg