Canonical Allele Identifier: CA414447351
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562010G>C , CM000685.2:g.139562010G>C GRCh38
NC_000023.10:g.138644169G>C , CM000685.1:g.138644169G>C GRCh37
NC_000023.9:g.138471835G>C NCBI36
NG_007994.1:g.36275G>C , LRG_556:g.36275G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1325G>C MANE Select ENSP00000218099.2:p.Gly442Ala
ENST00000643157.1:n.1723+269G>C
ENST00000218099.6:c.1325G>C ENSP00000218099.2:p.Gly442Ala
ENST00000394090.2:c.1211G>C ENSP00000377650.2:p.Gly404Ala
NM_000133.3:c.1325G>C , LRG_556t1:c.1325G>C NP_000124.1:p.Gly442Ala
NM_001313913.1:c.1211G>C NP_001300842.1:p.Gly404Ala
XM_005262397.3:c.1196G>C XP_005262454.1:p.Gly399Ala
XM_005262397.4:c.1196G>C XP_005262454.1:p.Gly399Ala
NM_000133.4:c.1325G>C MANE Select NP_000124.1:p.Gly442Ala
NM_001313913.2:c.1211G>C NP_001300842.1:p.Gly404Ala