Canonical Allele Identifier: CA2461407768
Gene: F9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139548361A= , CM000685.2:g.139548361A= GRCh38
NC_000023.10:g.138630520A= , CM000685.1:g.138630520A= GRCh37
NC_000023.9:g.138458186A= NCBI36
NG_007994.1:g.22626A= , LRG_556:g.22626A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.392-2A= MANE Select ENSP00000218099.2:n.392-2A=
ENST00000643157.1:n.1059-2A=
ENST00000218099.6:c.392-2A= ENSP00000218099.2:n.392-2A=
ENST00000394090.2:c.278-2A= ENSP00000377650.2:n.278-2A=
ENST00000479617.2:n.345-2A=
NM_000133.3:c.392-2A= , LRG_556t1:c.392-2A= NP_000124.1:n.392-2A=
NM_001313913.1:c.278-2A= NP_001300842.1:n.278-2A=
XM_005262397.3:c.392-2701A= XP_005262454.1:n.392-2701A=
XM_005262397.4:c.392-2701A= XP_005262454.1:n.392-2701A=
NM_000133.4:c.392-2A= MANE Select NP_000124.1:n.392-2A=
NM_001313913.2:c.278-2A= NP_001300842.1:n.278-2A=
Search 100 bp 5'
Search 100 bp 3'