Canonical Allele Identifier: CA414437635
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139541141T>G , CM000685.2:g.139541141T>G GRCh38
NC_000023.10:g.138623300T>G , CM000685.1:g.138623300T>G GRCh37
NC_000023.9:g.138450966T>G NCBI36
NG_007994.1:g.15406T>G , LRG_556:g.15406T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.343T>G MANE Select ENSP00000218099.2:p.Tyr115Asp
ENST00000218099.6:c.343T>G ENSP00000218099.2:p.Tyr115Asp
ENST00000394090.2:c.277+3755T>G ENSP00000377650.2:n.277+3755T>G
ENST00000479617.2:n.296T>G
NM_000133.3:c.343T>G , LRG_556t1:c.343T>G NP_000124.1:p.Tyr115Asp
NM_001313913.1:c.277+3755T>G NP_001300842.1:n.277+3755T>G
XM_005262397.3:c.343T>G XP_005262454.1:p.Tyr115Asp
XM_005262397.4:c.343T>G XP_005262454.1:p.Tyr115Asp
NM_000133.4:c.343T>G MANE Select NP_000124.1:p.Tyr115Asp
NM_001313913.2:c.277+3755T>G NP_001300842.1:n.277+3755T>G