Canonical Allele Identifier: CA414440608
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139551122C>G , CM000685.2:g.139551122C>G GRCh38
NC_000023.10:g.138633281C>G , CM000685.1:g.138633281C>G GRCh37
NC_000023.9:g.138460947C>G NCBI36
NG_007994.1:g.25387C>G , LRG_556:g.25387C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.581C>G MANE Select ENSP00000218099.2:p.Thr194Ser
ENST00000643157.1:n.1248C>G
ENST00000218099.6:c.581C>G ENSP00000218099.2:p.Thr194Ser
ENST00000394090.2:c.467C>G ENSP00000377650.2:p.Thr156Ser
NM_000133.3:c.581C>G , LRG_556t1:c.581C>G NP_000124.1:p.Thr194Ser
NM_001313913.1:c.467C>G NP_001300842.1:p.Thr156Ser
XM_005262397.3:c.452C>G XP_005262454.1:p.Thr151Ser
XM_005262397.4:c.452C>G XP_005262454.1:p.Thr151Ser
NM_000133.4:c.581C>G MANE Select NP_000124.1:p.Thr194Ser
NM_001313913.2:c.467C>G NP_001300842.1:p.Thr156Ser