Canonical Allele Identifier: CA2694839902
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562110A>G , CM000685.2:g.139562110A>G GRCh38
NC_000023.10:g.138644269A>G , CM000685.1:g.138644269A>G GRCh37
NC_000023.9:g.138471935A>G NCBI36
NG_007994.1:g.36375A>G , LRG_556:g.36375A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.*39A>G MANE Select ENSP00000218099.2:n.*39A>G
ENST00000643157.1:n.1723+369A>G
ENST00000218099.6:c.*39A>G ENSP00000218099.2:n.*39A>G
NM_000133.3:c.*39A>G , LRG_556t1:c.*39A>G NP_000124.1:n.*39A>G
NM_001313913.1:c.*39A>G NP_001300842.1:n.*39A>G
XM_005262397.3:c.*39A>G XP_005262454.1:n.*39A>G
XM_005262397.4:c.*39A>G XP_005262454.1:n.*39A>G
NM_000133.4:c.*39A>G MANE Select NP_000124.1:n.*39A>G
NM_001313913.2:c.*39A>G NP_001300842.1:n.*39A>G