Canonical Allele Identifier: CA2461412324
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562091G= , CM000685.2:g.139562091G= GRCh38
NC_000023.10:g.138644250G= , CM000685.1:g.138644250G= GRCh37
NC_000023.9:g.138471916G= NCBI36
NG_007994.1:g.36356G= , LRG_556:g.36356G=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.*20G= MANE Select ENSP00000218099.2:n.*20G=
ENST00000643157.1:n.1723+350G=
ENST00000218099.6:c.*20G= ENSP00000218099.2:n.*20G=
NM_000133.3:c.*20G= , LRG_556t1:c.*20G= NP_000124.1:n.*20G=
NM_001313913.1:c.*20G= NP_001300842.1:n.*20G=
XM_005262397.3:c.*20G= XP_005262454.1:n.*20G=
XM_005262397.4:c.*20G= XP_005262454.1:n.*20G=
NM_000133.4:c.*20G= MANE Select NP_000124.1:n.*20G=
NM_001313913.2:c.*20G= NP_001300842.1:n.*20G=