Canonical Allele Identifier: CA2694839875
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561461A>G , CM000685.2:g.139561461A>G GRCh38
NC_000023.10:g.138643620A>G , CM000685.1:g.138643620A>G GRCh37
NC_000023.9:g.138471286A>G NCBI36
NG_007994.1:g.35726A>G , LRG_556:g.35726A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.839-63A>G MANE Select ENSP00000218099.2:n.839-63A>G
ENST00000643157.1:n.1506-63A>G
ENST00000218099.6:c.839-63A>G ENSP00000218099.2:n.839-63A>G
ENST00000394090.2:c.725-63A>G ENSP00000377650.2:n.725-63A>G
NM_000133.3:c.839-63A>G , LRG_556t1:c.839-63A>G NP_000124.1:n.839-63A>G
NM_001313913.1:c.725-63A>G NP_001300842.1:n.725-63A>G
XM_005262397.3:c.710-63A>G XP_005262454.1:n.710-63A>G
XM_005262397.4:c.710-63A>G XP_005262454.1:n.710-63A>G
NM_000133.4:c.839-63A>G MANE Select NP_000124.1:n.839-63A>G
NM_001313913.2:c.725-63A>G NP_001300842.1:n.725-63A>G