Canonical Allele Identifier: CA557063144

Gene: F11

Linked Data

• dbSNP Id: rs1488138061
• gnomAD v2: 4-187187231-C-G
• gnomAD v3: 4-186266077-C-G
• gnomAD v4: 4-186266077-C-G
• MyVariant Identifiers: chr4:g.187187231C>G (hg19) ; chr4:g.186266077C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186266077C>G , CM000666.2:g.186266077C>G	GRCh38
NC_000004.11:g.187187231C>G , CM000666.1:g.187187231C>G	GRCh37
NC_000004.10:g.187424225C>G	NCBI36
NG_008051.1:g.5114C>G , LRG_583:g.5114C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.6:c.-220C>G	ENSP00000384957.2:n.-220C>G
NM_000128.3:c.-220C>G , LRG_583t1:c.-220C>G	NP_000119.1:n.-220C>G
XM_005262821.2:c.-220C>G	XP_005262878.1:n.-220C>G
XM_005262822.2:c.-220C>G	XP_005262879.1:n.-220C>G
XM_005262823.2:c.-220C>G	XP_005262880.1:n.-220C>G
XM_005262824.1:c.-220C>G	XP_005262881.1:n.-220C>G
XM_006714137.1:c.-220C>G	XP_006714200.1:n.-220C>G
XR_938706.1:n.133C>G
XR_938707.1:n.133C>G
NM_001354804.1:c.-220C>G	NP_001341733.1:n.-220C>G
XM_005262821.4:c.-220C>G	XP_005262878.1:n.-220C>G
XM_005262822.4:c.-220C>G	XP_005262879.1:n.-220C>G
XM_005262823.4:c.-220C>G	XP_005262880.1:n.-220C>G
XM_006714137.3:c.-220C>G	XP_006714200.1:n.-220C>G
XM_017007884.2:c.-220C>G	XP_016863373.1:n.-220C>G
XM_017007885.2:c.-220C>G	XP_016863374.1:n.-220C>G
XM_017007886.2:c.-220C>G	XP_016863375.1:n.-220C>G
XR_001741172.2:n.114C>G