Canonical Allele Identifier: CA442639139

Gene: F11

Linked Data

• dbSNP Id: rs1376309032
• MyVariant Identifiers: chr4:g.187205403C>T (hg19) ; chr4:g.186284249C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284249C>T , CM000666.2:g.186284249C>T	GRCh38
NC_000004.11:g.187205403C>T , CM000666.1:g.187205403C>T	GRCh37
NC_000004.10:g.187442397C>T	NCBI36
NG_008051.1:g.23286C>T , LRG_583:g.23286C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1293C>T MANE Select	ENSP00000384957.2:p.His431=
ENST00000264692.8:c.1131C>T	ENSP00000264692.5:p.His377=
ENST00000403665.6:c.1293C>T	ENSP00000384957.2:p.His431=
NM_000128.3:c.1293C>T , LRG_583t1:c.1293C>T	NP_000119.1:p.His431=
XM_005262821.2:c.1296C>T	XP_005262878.1:p.His432=
XM_005262822.2:c.1296C>T	XP_005262879.1:p.His432=
XM_005262823.2:c.1026C>T	XP_005262880.1:p.His342=
XM_005262824.1:c.1296C>T	XP_005262881.1:p.His432=
XM_006714137.1:c.1248C>T	XP_006714200.1:p.His416=
XR_938706.1:n.1701C>T
XR_938707.1:n.1701C>T
XM_005262821.4:c.1296C>T	XP_005262878.1:p.His432=
XM_005262822.4:c.1296C>T	XP_005262879.1:p.His432=
XM_005262823.4:c.1026C>T	XP_005262880.1:p.His342=
XM_006714137.3:c.1248C>T	XP_006714200.1:p.His416=
XR_001741172.2:n.1767C>T
NM_000128.4:c.1293C>T MANE Select	NP_000119.1:p.His431=