Canonical Allele Identifier: CA414447545
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562045A>T , CM000685.2:g.139562045A>T GRCh38
NC_000023.10:g.138644204A>T , CM000685.1:g.138644204A>T GRCh37
NC_000023.9:g.138471870A>T NCBI36
NG_007994.1:g.36310A>T , LRG_556:g.36310A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1360A>T MANE Select ENSP00000218099.2:p.Ile454Phe
ENST00000643157.1:n.1723+304A>T
ENST00000218099.6:c.1360A>T ENSP00000218099.2:p.Ile454Phe
ENST00000394090.2:c.1246A>T ENSP00000377650.2:p.Ile416Phe
NM_000133.3:c.1360A>T , LRG_556t1:c.1360A>T NP_000124.1:p.Ile454Phe
NM_001313913.1:c.1246A>T NP_001300842.1:p.Ile416Phe
XM_005262397.3:c.1231A>T XP_005262454.1:p.Ile411Phe
XM_005262397.4:c.1231A>T XP_005262454.1:p.Ile411Phe
NM_000133.4:c.1360A>T MANE Select NP_000124.1:p.Ile454Phe
NM_001313913.2:c.1246A>T NP_001300842.1:p.Ile416Phe