Canonical Allele Identifier: CA414447580
Gene: F9 HGNC NCBI

Linked Data

dbSNP Id: rs1928134057

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562051G>A , CM000685.2:g.139562051G>A GRCh38
NC_000023.10:g.138644210G>A , CM000685.1:g.138644210G>A GRCh37
NC_000023.9:g.138471876G>A NCBI36
NG_007994.1:g.36316G>A , LRG_556:g.36316G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1366G>A MANE Select ENSP00000218099.2:p.Glu456Lys
ENST00000643157.1:n.1723+310G>A
ENST00000218099.6:c.1366G>A ENSP00000218099.2:p.Glu456Lys
ENST00000394090.2:c.1252G>A ENSP00000377650.2:p.Glu418Lys
NM_000133.3:c.1366G>A , LRG_556t1:c.1366G>A NP_000124.1:p.Glu456Lys
NM_001313913.1:c.1252G>A NP_001300842.1:p.Glu418Lys
XM_005262397.3:c.1237G>A XP_005262454.1:p.Glu413Lys
XM_005262397.4:c.1237G>A XP_005262454.1:p.Glu413Lys
NM_000133.4:c.1366G>A MANE Select NP_000124.1:p.Glu456Lys
NM_001313913.2:c.1252G>A NP_001300842.1:p.Glu418Lys