Canonical Allele Identifier: CA3163748
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs779432573

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276330A>G , CM000666.2:g.186276330A>G GRCh38
NC_000004.11:g.187197484A>G , CM000666.1:g.187197484A>G GRCh37
NC_000004.10:g.187434478A>G NCBI36
NG_008051.1:g.15367A>G , LRG_583:g.15367A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.695A>G MANE Select ENSP00000384957.2:p.His232Arg
ENST00000264692.8:c.533A>G ENSP00000264692.5:p.His178Arg
ENST00000403665.6:c.695A>G ENSP00000384957.2:p.His232Arg
ENST00000452239.1:c.142A>G
NM_000128.3:c.695A>G , LRG_583t1:c.695A>G NP_000119.1:p.His232Arg
XM_005262821.2:c.695A>G XP_005262878.1:p.His232Arg
XM_005262822.2:c.695A>G XP_005262879.1:p.His232Arg
XM_005262823.2:c.485+2055A>G XP_005262880.1:n.485+2055A>G
XM_005262824.1:c.695A>G XP_005262881.1:p.His232Arg
XM_006714137.1:c.695A>G XP_006714200.1:p.His232Arg
XR_938706.1:n.1047A>G
XR_938707.1:n.1047A>G
XM_005262821.4:c.695A>G XP_005262878.1:p.His232Arg
XM_005262822.4:c.695A>G XP_005262879.1:p.His232Arg
XM_005262823.4:c.485+2055A>G XP_005262880.1:n.485+2055A>G
XM_006714137.3:c.695A>G XP_006714200.1:p.His232Arg
XM_017007884.2:c.695A>G XP_016863373.1:p.His232Arg
XM_017007885.2:c.695A>G XP_016863374.1:p.His232Arg
XM_017007886.2:c.695A>G XP_016863375.1:p.His232Arg
XR_001741172.2:n.1028A>G
NM_000128.4:c.695A>G MANE Select NP_000119.1:p.His232Arg