Canonical Allele Identifier: CA2461412066
Gene: F9 HGNC NCBI

Linked Data

dbSNP Id: rs1289561391

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561521T>G , CM000685.2:g.139561521T>G GRCh38
NC_000023.10:g.138643680T>G , CM000685.1:g.138643680T>G GRCh37
NC_000023.9:g.138471346T>G NCBI36
NG_007994.1:g.35786T>G , LRG_556:g.35786T>G

Transcript Alleles

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