Canonical Allele Identifier: CA557063142

Gene: F11

Linked Data

• ClinVar Variation Id: 899920
• ClinVar RCV Id: RCV001144806
• dbSNP Id: rs1263431242
• gnomAD v2: 4-187187218-C-T
• gnomAD v3: 4-186266064-C-T
• gnomAD v4: 4-186266064-C-T
• MyVariant Identifiers: chr4:g.187187218C>T (hg19) ; chr4:g.186266064C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186266064C>T , CM000666.2:g.186266064C>T	GRCh38
NC_000004.11:g.187187218C>T , CM000666.1:g.187187218C>T	GRCh37
NC_000004.10:g.187424212C>T	NCBI36
NG_008051.1:g.5101C>T , LRG_583:g.5101C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.6:c.-233C>T	ENSP00000384957.2:n.-233C>T
NM_000128.3:c.-233C>T , LRG_583t1:c.-233C>T	NP_000119.1:n.-233C>T
XM_005262821.2:c.-233C>T	XP_005262878.1:n.-233C>T
XM_005262822.2:c.-233C>T	XP_005262879.1:n.-233C>T
XM_005262823.2:c.-233C>T	XP_005262880.1:n.-233C>T
XM_005262824.1:c.-233C>T	XP_005262881.1:n.-233C>T
XM_006714137.1:c.-233C>T	XP_006714200.1:n.-233C>T
XR_938706.1:n.120C>T
XR_938707.1:n.120C>T
NM_001354804.1:c.-233C>T	NP_001341733.1:n.-233C>T
XM_005262821.4:c.-233C>T	XP_005262878.1:n.-233C>T
XM_005262822.4:c.-233C>T	XP_005262879.1:n.-233C>T
XM_005262823.4:c.-233C>T	XP_005262880.1:n.-233C>T
XM_006714137.3:c.-233C>T	XP_006714200.1:n.-233C>T
XM_017007884.2:c.-233C>T	XP_016863373.1:n.-233C>T
XM_017007885.2:c.-233C>T	XP_016863374.1:n.-233C>T
XM_017007886.2:c.-233C>T	XP_016863375.1:n.-233C>T
XR_001741172.2:n.101C>T