Canonical Allele Identifier: CA2516103856
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561482G>T , CM000685.2:g.139561482G>T GRCh38
NC_000023.10:g.138643641G>T , CM000685.1:g.138643641G>T GRCh37
NC_000023.9:g.138471307G>T NCBI36
NG_007994.1:g.35747G>T , LRG_556:g.35747G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.839-42G>T MANE Select ENSP00000218099.2:n.839-42G>T
ENST00000643157.1:n.1506-42G>T
ENST00000218099.6:c.839-42G>T ENSP00000218099.2:n.839-42G>T
ENST00000394090.2:c.725-42G>T ENSP00000377650.2:n.725-42G>T
NM_000133.3:c.839-42G>T , LRG_556t1:c.839-42G>T NP_000124.1:n.839-42G>T
NM_001313913.1:c.725-42G>T NP_001300842.1:n.725-42G>T
XM_005262397.3:c.710-42G>T XP_005262454.1:n.710-42G>T
XM_005262397.4:c.710-42G>T XP_005262454.1:n.710-42G>T
NM_000133.4:c.839-42G>T MANE Select NP_000124.1:n.839-42G>T
NM_001313913.2:c.725-42G>T NP_001300842.1:n.725-42G>T