Canonical Allele Identifier: CA414446933
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561947G>T , CM000685.2:g.139561947G>T GRCh38
NC_000023.10:g.138644106G>T , CM000685.1:g.138644106G>T GRCh37
NC_000023.9:g.138471772G>T NCBI36
NG_007994.1:g.36212G>T , LRG_556:g.36212G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1262G>T MANE Select ENSP00000218099.2:p.Gly421Val
ENST00000643157.1:n.1723+206G>T
ENST00000218099.6:c.1262G>T ENSP00000218099.2:p.Gly421Val
ENST00000394090.2:c.1148G>T ENSP00000377650.2:p.Gly383Val
NM_000133.3:c.1262G>T , LRG_556t1:c.1262G>T NP_000124.1:p.Gly421Val
NM_001313913.1:c.1148G>T NP_001300842.1:p.Gly383Val
XM_005262397.3:c.1133G>T XP_005262454.1:p.Gly378Val
XM_005262397.4:c.1133G>T XP_005262454.1:p.Gly378Val
NM_000133.4:c.1262G>T MANE Select NP_000124.1:p.Gly421Val
NM_001313913.2:c.1148G>T NP_001300842.1:p.Gly383Val