Canonical Allele Identifier: CA16040943
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 370695
dbSNP Id: rs1057516695

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186275785A>G , CM000666.2:g.186275785A>G GRCh38
NC_000004.11:g.187196939A>G , CM000666.1:g.187196939A>G GRCh37
NC_000004.10:g.187433933A>G NCBI36
NG_008051.1:g.14822A>G , LRG_583:g.14822A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.486-2A>G MANE Select ENSP00000384957.2:n.486-2A>G
ENST00000264692.8:c.324-2A>G ENSP00000264692.5:n.324-2A>G
ENST00000403665.6:c.486-2A>G ENSP00000384957.2:n.486-2A>G
NM_000128.3:c.486-2A>G , LRG_583t1:c.486-2A>G NP_000119.1:n.486-2A>G
XM_005262821.2:c.486-2A>G XP_005262878.1:n.486-2A>G
XM_005262822.2:c.486-2A>G XP_005262879.1:n.486-2A>G
XM_005262823.2:c.485+1510A>G XP_005262880.1:n.485+1510A>G
XM_005262824.1:c.486-2A>G XP_005262881.1:n.486-2A>G
XM_006714137.1:c.486-2A>G XP_006714200.1:n.486-2A>G
XR_938706.1:n.838-2A>G
XR_938707.1:n.838-2A>G
XM_005262821.4:c.486-2A>G XP_005262878.1:n.486-2A>G
XM_005262822.4:c.486-2A>G XP_005262879.1:n.486-2A>G
XM_005262823.4:c.485+1510A>G XP_005262880.1:n.485+1510A>G
XM_006714137.3:c.486-2A>G XP_006714200.1:n.486-2A>G
XM_017007884.2:c.486-2A>G XP_016863373.1:n.486-2A>G
XM_017007885.2:c.486-2A>G XP_016863374.1:n.486-2A>G
XM_017007886.2:c.486-2A>G XP_016863375.1:n.486-2A>G
XR_001741172.2:n.819-2A>G
NM_000128.4:c.486-2A>G MANE Select NP_000119.1:n.486-2A>G