Canonical Allele Identifier: CA442639074

Gene: F11

Linked Data

• dbSNP Id: rs2094223399
• gnomAD v3: 4-186284198-C-T
• gnomAD v4: 4-186284198-C-T
• MyVariant Identifiers: chr4:g.187205352C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284198C>T , CM000666.2:g.186284198C>T	GRCh38
NC_000004.11:g.187205352C>T , CM000666.1:g.187205352C>T	GRCh37
NC_000004.10:g.187442346C>T	NCBI36
NG_008051.1:g.23235C>T , LRG_583:g.23235C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1242C>T MANE Select	ENSP00000384957.2:p.His414=
ENST00000264692.8:c.1080C>T	ENSP00000264692.5:p.His360=
ENST00000403665.6:c.1242C>T	ENSP00000384957.2:p.His414=
NM_000128.3:c.1242C>T , LRG_583t1:c.1242C>T	NP_000119.1:p.His414=
XM_005262821.2:c.1245C>T	XP_005262878.1:p.His415=
XM_005262822.2:c.1245C>T	XP_005262879.1:p.His415=
XM_005262823.2:c.975C>T	XP_005262880.1:p.His325=
XM_005262824.1:c.1245C>T	XP_005262881.1:p.His415=
XM_006714137.1:c.1197C>T	XP_006714200.1:p.His399=
XR_938706.1:n.1650C>T
XR_938707.1:n.1650C>T
XM_005262821.4:c.1245C>T	XP_005262878.1:p.His415=
XM_005262822.4:c.1245C>T	XP_005262879.1:p.His415=
XM_005262823.4:c.975C>T	XP_005262880.1:p.His325=
XM_006714137.3:c.1197C>T	XP_006714200.1:p.His399=
XR_001741172.2:n.1716C>T
NM_000128.4:c.1242C>T MANE Select	NP_000119.1:p.His414=