Canonical Allele Identifier: CA256461763

Gene: F7

Linked Data

• dbSNP Id: rs868287262
• MyVariant Identifiers: chr13:g.113773046G>A (hg19) ; chr13:g.113118732G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118732G>A , CM000675.2:g.113118732G>A	GRCh38
NC_000013.10:g.113773046G>A , CM000675.1:g.113773046G>A	GRCh37
NC_000013.9:g.112821047G>A	NCBI36
NG_009258.1:g.934G>A , LRG_548:g.934G>A
NG_009262.1:g.17942G>A , LRG_554:g.17942G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1059G>A MANE Select	ENSP00000329546.4:p.Arg353=
ENST00000346342.7:c.1059G>A	ENSP00000329546.3:p.Arg353=
ENST00000375581.3:c.1125G>A	ENSP00000364731.3:p.Arg375=
ENST00000541084.5:c.873G>A	ENSP00000442051.2:p.Arg291=
NM_000131.4:c.1125G>A , LRG_554t1:c.1125G>A	NP_000122.1:p.Arg375=
NM_001267554.1:c.873G>A	NP_001254483.1:p.Arg291=
NM_019616.3:c.1059G>A , LRG_554t2:c.1059G>A	NP_062562.1:p.Arg353=
NR_051961.1:n.1146G>A
XM_006719963.2:c.918G>A	XP_006720026.1:p.Arg306=
XM_011537474.1:c.1167G>A	XP_011535776.1:p.Arg389=
XM_011537475.1:c.981G>A	XP_011535777.1:p.Arg327=
XM_011537476.1:c.819G>A	XP_011535778.1:p.Arg273=
XM_011537477.1:c.1128G>A	XP_011535779.1:p.Arg376=
XM_006719963.3:c.963G>A	XP_006720026.2:p.Arg321=
XM_011537474.2:c.1212G>A	XP_011535776.2:p.Arg404=
XM_011537475.2:c.1026G>A	XP_011535777.2:p.Arg342=
XM_011537476.2:c.819G>A	XP_011535778.1:p.Arg273=
NM_019616.4:c.1059G>A MANE Select	NP_062562.1:p.Arg353=
NR_051961.2:n.1143G>A
NM_001267554.2:c.873G>A	NP_001254483.1:p.Arg291=