Canonical Allele Identifier: CA518864344
Gene: F9 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.138644212A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562053A>G , CM000685.2:g.139562053A>G GRCh38
NC_000023.10:g.138644212A>G , CM000685.1:g.138644212A>G GRCh37
NC_000023.9:g.138471878A>G NCBI36
NG_007994.1:g.36318A>G , LRG_556:g.36318A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1368A>G MANE Select ENSP00000218099.2:p.Glu456=
ENST00000643157.1:n.1723+312A>G
ENST00000218099.6:c.1368A>G ENSP00000218099.2:p.Glu456=
ENST00000394090.2:c.1254A>G ENSP00000377650.2:p.Glu418=
NM_000133.3:c.1368A>G , LRG_556t1:c.1368A>G NP_000124.1:p.Glu456=
NM_001313913.1:c.1254A>G NP_001300842.1:p.Glu418=
XM_005262397.3:c.1239A>G XP_005262454.1:p.Glu413=
XM_005262397.4:c.1239A>G XP_005262454.1:p.Glu413=
NM_000133.4:c.1368A>G MANE Select NP_000124.1:p.Glu456=
NM_001313913.2:c.1254A>G NP_001300842.1:p.Glu418=