Canonical Allele Identifier: CA414445488
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561717C>G , CM000685.2:g.139561717C>G GRCh38
NC_000023.10:g.138643876C>G , CM000685.1:g.138643876C>G GRCh37
NC_000023.9:g.138471542C>G NCBI36
NG_007994.1:g.35982C>G , LRG_556:g.35982C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1032C>G MANE Select ENSP00000218099.2:p.Ile344Met
ENST00000643157.1:n.1699C>G
ENST00000218099.6:c.1032C>G ENSP00000218099.2:p.Ile344Met
ENST00000394090.2:c.918C>G ENSP00000377650.2:p.Ile306Met
NM_000133.3:c.1032C>G , LRG_556t1:c.1032C>G NP_000124.1:p.Ile344Met
NM_001313913.1:c.918C>G NP_001300842.1:p.Ile306Met
XM_005262397.3:c.903C>G XP_005262454.1:p.Ile301Met
XM_005262397.4:c.903C>G XP_005262454.1:p.Ile301Met
NM_000133.4:c.1032C>G MANE Select NP_000124.1:p.Ile344Met
NM_001313913.2:c.918C>G NP_001300842.1:p.Ile306Met