Canonical Allele Identifier: CA414446961
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561953G>A , CM000685.2:g.139561953G>A GRCh38
NC_000023.10:g.138644112G>A , CM000685.1:g.138644112G>A GRCh37
NC_000023.9:g.138471778G>A NCBI36
NG_007994.1:g.36218G>A , LRG_556:g.36218G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1268G>A MANE Select ENSP00000218099.2:p.Ser423Asn
ENST00000643157.1:n.1723+212G>A
ENST00000218099.6:c.1268G>A ENSP00000218099.2:p.Ser423Asn
ENST00000394090.2:c.1154G>A ENSP00000377650.2:p.Ser385Asn
NM_000133.3:c.1268G>A , LRG_556t1:c.1268G>A NP_000124.1:p.Ser423Asn
NM_001313913.1:c.1154G>A NP_001300842.1:p.Ser385Asn
XM_005262397.3:c.1139G>A XP_005262454.1:p.Ser380Asn
XM_005262397.4:c.1139G>A XP_005262454.1:p.Ser380Asn
NM_000133.4:c.1268G>A MANE Select NP_000124.1:p.Ser423Asn
NM_001313913.2:c.1154G>A NP_001300842.1:p.Ser385Asn