Canonical Allele Identifier: CA256461637

Gene: F7

Linked Data

• dbSNP Id: rs202240468
• MyVariant Identifiers: chr13:g.113772917G>T (hg19) ; chr13:g.113118603G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118603G>T , CM000675.2:g.113118603G>T	GRCh38
NC_000013.10:g.113772917G>T , CM000675.1:g.113772917G>T	GRCh37
NC_000013.9:g.112820918G>T	NCBI36
NG_009258.1:g.805G>T , LRG_548:g.805G>T
NG_009262.1:g.17813G>T , LRG_554:g.17813G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.930G>T MANE Select	ENSP00000329546.4:p.Thr310=
ENST00000346342.7:c.930G>T	ENSP00000329546.3:p.Thr310=
ENST00000375581.3:c.996G>T	ENSP00000364731.3:p.Thr332=
ENST00000541084.5:c.744G>T	ENSP00000442051.2:p.Thr248=
NM_000131.4:c.996G>T , LRG_554t1:c.996G>T	NP_000122.1:p.Thr332=
NM_001267554.1:c.744G>T	NP_001254483.1:p.Thr248=
NM_019616.3:c.930G>T , LRG_554t2:c.930G>T	NP_062562.1:p.Thr310=
NR_051961.1:n.1017G>T
XM_006719963.2:c.789G>T	XP_006720026.1:p.Thr263=
XM_011537474.1:c.1038G>T	XP_011535776.1:p.Thr346=
XM_011537475.1:c.852G>T	XP_011535777.1:p.Thr284=
XM_011537476.1:c.690G>T	XP_011535778.1:p.Thr230=
XM_011537477.1:c.999G>T	XP_011535779.1:p.Thr333=
XM_006719963.3:c.834G>T	XP_006720026.2:p.Thr278=
XM_011537474.2:c.1083G>T	XP_011535776.2:p.Thr361=
XM_011537475.2:c.897G>T	XP_011535777.2:p.Thr299=
XM_011537476.2:c.690G>T	XP_011535778.1:p.Thr230=
NM_019616.4:c.930G>T MANE Select	NP_062562.1:p.Thr310=
NR_051961.2:n.1014G>T
NM_001267554.2:c.744G>T	NP_001254483.1:p.Thr248=