Canonical Allele Identifier: CA792315574

Gene: F11

Linked Data

• dbSNP Id: rs1456050107
• gnomAD v3: 4-186285851-T-G
• gnomAD v4: 4-186285851-T-G
• MyVariant Identifiers: chr4:g.187207005T>G (hg19) ; chr4:g.186285851T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285851T>G , CM000666.2:g.186285851T>G	GRCh38
NC_000004.11:g.187207005T>G , CM000666.1:g.187207005T>G	GRCh37
NC_000004.10:g.187443999T>G	NCBI36
NG_008051.1:g.24888T>G , LRG_583:g.24888T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1480+38T>G MANE Select	ENSP00000384957.2:n.1480+38T>G
ENST00000264691.4:c.176+38T>G
ENST00000264692.8:c.1318+38T>G	ENSP00000264692.5:n.1318+38T>G
ENST00000403665.6:c.1480+38T>G	ENSP00000384957.2:n.1480+38T>G
NM_000128.3:c.1480+38T>G , LRG_583t1:c.1480+38T>G	NP_000119.1:n.1480+38T>G
XM_005262821.2:c.1483+38T>G	XP_005262878.1:n.1483+38T>G
XM_005262822.2:c.1483+38T>G	XP_005262879.1:n.1483+38T>G
XM_005262823.2:c.1213+38T>G	XP_005262880.1:n.1213+38T>G
XM_005262824.1:c.1483+38T>G	XP_005262881.1:n.1483+38T>G
XM_006714137.1:c.1435+38T>G	XP_006714200.1:n.1435+38T>G
XR_938706.1:n.1888+38T>G
XR_938707.1:n.1888+38T>G
XM_005262821.4:c.1483+38T>G	XP_005262878.1:n.1483+38T>G
XM_005262822.4:c.1483+38T>G	XP_005262879.1:n.1483+38T>G
XM_005262823.4:c.1213+38T>G	XP_005262880.1:n.1213+38T>G
XM_006714137.3:c.1435+38T>G	XP_006714200.1:n.1435+38T>G
XR_001741172.2:n.1954+38T>G
NM_000128.4:c.1480+38T>G MANE Select	NP_000119.1:n.1480+38T>G