Canonical Allele Identifier: CA414444402
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561524G>C , CM000685.2:g.139561524G>C GRCh38
NC_000023.10:g.138643683G>C , CM000685.1:g.138643683G>C GRCh37
NC_000023.9:g.138471349G>C NCBI36
NG_007994.1:g.35789G>C , LRG_556:g.35789G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.839G>C MANE Select ENSP00000218099.2:p.Gly280Ala
ENST00000643157.1:n.1506G>C
ENST00000218099.6:c.839G>C ENSP00000218099.2:p.Gly280Ala
ENST00000394090.2:c.725G>C ENSP00000377650.2:p.Gly242Ala
NM_000133.3:c.839G>C , LRG_556t1:c.839G>C NP_000124.1:p.Gly280Ala
NM_001313913.1:c.725G>C NP_001300842.1:p.Gly242Ala
XM_005262397.3:c.710G>C XP_005262454.1:p.Gly237Ala
XM_005262397.4:c.710G>C XP_005262454.1:p.Gly237Ala
NM_000133.4:c.839G>C MANE Select NP_000124.1:p.Gly280Ala
NM_001313913.2:c.725G>C NP_001300842.1:p.Gly242Ala