Canonical Allele Identifier: CA414447498
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562037T>G , CM000685.2:g.139562037T>G GRCh38
NC_000023.10:g.138644196T>G , CM000685.1:g.138644196T>G GRCh37
NC_000023.9:g.138471862T>G NCBI36
NG_007994.1:g.36302T>G , LRG_556:g.36302T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.1352T>G MANE Select ENSP00000218099.2:p.Val451Gly
ENST00000643157.1:n.1723+296T>G
ENST00000218099.6:c.1352T>G ENSP00000218099.2:p.Val451Gly
ENST00000394090.2:c.1238T>G ENSP00000377650.2:p.Val413Gly
NM_000133.3:c.1352T>G , LRG_556t1:c.1352T>G NP_000124.1:p.Val451Gly
NM_001313913.1:c.1238T>G NP_001300842.1:p.Val413Gly
XM_005262397.3:c.1223T>G XP_005262454.1:p.Val408Gly
XM_005262397.4:c.1223T>G XP_005262454.1:p.Val408Gly
NM_000133.4:c.1352T>G MANE Select NP_000124.1:p.Val451Gly
NM_001313913.2:c.1238T>G NP_001300842.1:p.Val413Gly