Canonical Allele Identifier: CA358942157

Gene: F11

Linked Data

• dbSNP Id: rs1265867958
• gnomAD v3: 4-186284227-A-G
• gnomAD v4: 4-186284227-A-G
• MyVariant Identifiers: chr4:g.187205381A>G (hg19) ; chr4:g.186284227A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284227A>G , CM000666.2:g.186284227A>G	GRCh38
NC_000004.11:g.187205381A>G , CM000666.1:g.187205381A>G	GRCh37
NC_000004.10:g.187442375A>G	NCBI36
NG_008051.1:g.23264A>G , LRG_583:g.23264A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1271A>G MANE Select	ENSP00000384957.2:p.Gln424Arg
ENST00000264692.8:c.1109A>G	ENSP00000264692.5:p.Gln370Arg
ENST00000403665.6:c.1271A>G	ENSP00000384957.2:p.Gln424Arg
NM_000128.3:c.1271A>G , LRG_583t1:c.1271A>G	NP_000119.1:p.Gln424Arg
XM_005262821.2:c.1274A>G	XP_005262878.1:p.Gln425Arg
XM_005262822.2:c.1274A>G	XP_005262879.1:p.Gln425Arg
XM_005262823.2:c.1004A>G	XP_005262880.1:p.Gln335Arg
XM_005262824.1:c.1274A>G	XP_005262881.1:p.Gln425Arg
XM_006714137.1:c.1226A>G	XP_006714200.1:p.Gln409Arg
XR_938706.1:n.1679A>G
XR_938707.1:n.1679A>G
XM_005262821.4:c.1274A>G	XP_005262878.1:p.Gln425Arg
XM_005262822.4:c.1274A>G	XP_005262879.1:p.Gln425Arg
XM_005262823.4:c.1004A>G	XP_005262880.1:p.Gln335Arg
XM_006714137.3:c.1226A>G	XP_006714200.1:p.Gln409Arg
XR_001741172.2:n.1745A>G
NM_000128.4:c.1271A>G MANE Select	NP_000119.1:p.Gln424Arg