Canonical Allele Identifier: CA3039260804
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561494G>A , CM000685.2:g.139561494G>A GRCh38
NC_000023.10:g.138643653G>A , CM000685.1:g.138643653G>A GRCh37
NC_000023.9:g.138471319G>A NCBI36
NG_007994.1:g.35759G>A , LRG_556:g.35759G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.839-30G>A MANE Select ENSP00000218099.2:n.839-30G>A
ENST00000643157.1:n.1506-30G>A
ENST00000218099.6:c.839-30G>A ENSP00000218099.2:n.839-30G>A
ENST00000394090.2:c.725-30G>A ENSP00000377650.2:n.725-30G>A
NM_000133.3:c.839-30G>A , LRG_556t1:c.839-30G>A NP_000124.1:n.839-30G>A
NM_001313913.1:c.725-30G>A NP_001300842.1:n.725-30G>A
XM_005262397.3:c.710-30G>A XP_005262454.1:n.710-30G>A
XM_005262397.4:c.710-30G>A XP_005262454.1:n.710-30G>A
NM_000133.4:c.839-30G>A MANE Select NP_000124.1:n.839-30G>A
NM_001313913.2:c.725-30G>A NP_001300842.1:n.725-30G>A