Canonical Allele Identifier: CA557396099

Gene: F11

Linked Data

• dbSNP Id: rs1231923407
• gnomAD v2: 4-187201542-A-G
• gnomAD v4: 4-186280388-A-G
• MyVariant Identifiers: chr4:g.187201542A>G (hg19) ; chr4:g.186280388A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280388A>G , CM000666.2:g.186280388A>G	GRCh38
NC_000004.11:g.187201542A>G , CM000666.1:g.187201542A>G	GRCh37
NC_000004.10:g.187438536A>G	NCBI36
NG_008051.1:g.19425A>G , LRG_583:g.19425A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1028+3A>G MANE Select	ENSP00000384957.2:n.1028+3A>G
ENST00000264692.8:c.866+3A>G	ENSP00000264692.5:n.866+3A>G
ENST00000403665.6:c.1028+3A>G	ENSP00000384957.2:n.1028+3A>G
ENST00000452239.1:c.475+3A>G
NM_000128.3:c.1028+3A>G , LRG_583t1:c.1028+3A>G	NP_000119.1:n.1028+3A>G
XM_005262821.2:c.1028+3A>G	XP_005262878.1:n.1028+3A>G
XM_005262822.2:c.1028+3A>G	XP_005262879.1:n.1028+3A>G
XM_005262823.2:c.758+3A>G	XP_005262880.1:n.758+3A>G
XM_005262824.1:c.1028+3A>G	XP_005262881.1:n.1028+3A>G
XM_006714137.1:c.980+3A>G	XP_006714200.1:n.980+3A>G
XR_938706.1:n.1380+3A>G
XR_938707.1:n.1380+3A>G
XM_005262821.4:c.1028+3A>G	XP_005262878.1:n.1028+3A>G
XM_005262822.4:c.1028+3A>G	XP_005262879.1:n.1028+3A>G
XM_005262823.4:c.758+3A>G	XP_005262880.1:n.758+3A>G
XM_006714137.3:c.980+3A>G	XP_006714200.1:n.980+3A>G
XM_017007884.2:c.1028+3A>G	XP_016863373.1:n.1028+3A>G
XM_017007885.2:c.1028+3A>G	XP_016863374.1:n.1028+3A>G
XM_017007886.2:c.1028+3A>G	XP_016863375.1:n.1028+3A>G
XR_001741172.2:n.1364A>G
NM_000128.4:c.1028+3A>G MANE Select	NP_000119.1:n.1028+3A>G