Canonical Allele Identifier: CA255363
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10599
ClinVar RCV Id: RCV000011345
dbSNP Id: rs137852246

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139560821T>G , CM000685.2:g.139560821T>G GRCh38
NC_000023.10:g.138642980T>G , CM000685.1:g.138642980T>G GRCh37
NC_000023.9:g.138470646T>G NCBI36
NG_007994.1:g.35086T>G , LRG_556:g.35086T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.804T>G MANE Select ENSP00000218099.2:p.Cys268Trp
ENST00000643157.1:n.1471T>G
ENST00000218099.6:c.804T>G ENSP00000218099.2:p.Cys268Trp
ENST00000394090.2:n.690T>G ENSP00000377650.2:p.Cys230Trp
NM_000133.3:c.804T>G , LRG_556t1:c.804T>G NP_000124.1:p.Cys268Trp
NM_001313913.1:c.690T>G NP_001300842.1:p.Cys230Trp
XM_005262397.3:c.675T>G XP_005262454.1:p.Cys225Trp
XM_005262397.4:c.675T>G XP_005262454.1:p.Cys225Trp
NM_000133.4:c.804T>G MANE Select NP_000124.1:p.Cys268Trp
NM_001313913.2:c.690T>G NP_001300842.1:p.Cys230Trp