Canonical Allele Identifier: CA557055432

Gene: F11

Linked Data

• dbSNP Id: rs1257160702
• gnomAD v2: 4-187206762-A-G
• gnomAD v4: 4-186285608-A-G
• MyVariant Identifiers: chr4:g.187206762A>G (hg19) ; chr4:g.186285608A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285608A>G , CM000666.2:g.186285608A>G	GRCh38
NC_000004.11:g.187206762A>G , CM000666.1:g.187206762A>G	GRCh37
NC_000004.10:g.187443756A>G	NCBI36
NG_008051.1:g.24645A>G , LRG_583:g.24645A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1305-30A>G MANE Select	ENSP00000384957.2:n.1305-30A>G
ENST00000264692.8:c.1143-30A>G	ENSP00000264692.5:n.1143-30A>G
ENST00000403665.6:c.1305-30A>G	ENSP00000384957.2:n.1305-30A>G
NM_000128.3:c.1305-30A>G , LRG_583t1:c.1305-30A>G	NP_000119.1:n.1305-30A>G
XM_005262821.2:c.1308-30A>G	XP_005262878.1:n.1308-30A>G
XM_005262822.2:c.1308-30A>G	XP_005262879.1:n.1308-30A>G
XM_005262823.2:c.1038-30A>G	XP_005262880.1:n.1038-30A>G
XM_005262824.1:c.1308-30A>G	XP_005262881.1:n.1308-30A>G
XM_006714137.1:c.1260-30A>G	XP_006714200.1:n.1260-30A>G
XR_938706.1:n.1713-30A>G
XR_938707.1:n.1713-30A>G
XM_005262821.4:c.1308-30A>G	XP_005262878.1:n.1308-30A>G
XM_005262822.4:c.1308-30A>G	XP_005262879.1:n.1308-30A>G
XM_005262823.4:c.1038-30A>G	XP_005262880.1:n.1038-30A>G
XM_006714137.3:c.1260-30A>G	XP_006714200.1:n.1260-30A>G
XR_001741172.2:n.1779-30A>G
NM_000128.4:c.1305-30A>G MANE Select	NP_000119.1:n.1305-30A>G