Canonical Allele Identifier: CA414444438
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561530A>C , CM000685.2:g.139561530A>C GRCh38
NC_000023.10:g.138643689A>C , CM000685.1:g.138643689A>C GRCh37
NC_000023.9:g.138471355A>C NCBI36
NG_007994.1:g.35795A>C , LRG_556:g.35795A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.845A>C MANE Select ENSP00000218099.2:p.His282Pro
ENST00000643157.1:n.1512A>C
ENST00000218099.6:c.845A>C ENSP00000218099.2:p.His282Pro
ENST00000394090.2:c.731A>C ENSP00000377650.2:p.His244Pro
NM_000133.3:c.845A>C , LRG_556t1:c.845A>C NP_000124.1:p.His282Pro
NM_001313913.1:c.731A>C NP_001300842.1:p.His244Pro
XM_005262397.3:c.716A>C XP_005262454.1:p.His239Pro
XM_005262397.4:c.716A>C XP_005262454.1:p.His239Pro
NM_000133.4:c.845A>C MANE Select NP_000124.1:p.His282Pro
NM_001313913.2:c.731A>C NP_001300842.1:p.His244Pro