Canonical Allele Identifier: CA485423890

Gene: F7

Linked Data

• dbSNP Id: rs1365354034
• MyVariant Identifiers: chr13:g.113772857G>A (hg19) ; chr13:g.113118543G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118543G>A , CM000675.2:g.113118543G>A	GRCh38
NC_000013.10:g.113772857G>A , CM000675.1:g.113772857G>A	GRCh37
NC_000013.9:g.112820858G>A	NCBI36
NG_009258.1:g.745G>A , LRG_548:g.745G>A
NG_009262.1:g.17753G>A , LRG_554:g.17753G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.870G>A MANE Select	ENSP00000329546.4:p.Val290=
ENST00000346342.7:c.870G>A	ENSP00000329546.3:p.Val290=
ENST00000375581.3:c.936G>A	ENSP00000364731.3:p.Val312=
ENST00000541084.5:c.684G>A	ENSP00000442051.2:p.Val228=
NM_000131.4:c.936G>A , LRG_554t1:c.936G>A	NP_000122.1:p.Val312=
NM_001267554.1:c.684G>A	NP_001254483.1:p.Val228=
NM_019616.3:c.870G>A , LRG_554t2:c.870G>A	NP_062562.1:p.Val290=
NR_051961.1:n.957G>A
XM_006719963.2:c.729G>A	XP_006720026.1:p.Val243=
XM_011537474.1:c.978G>A	XP_011535776.1:p.Val326=
XM_011537475.1:c.792G>A	XP_011535777.1:p.Val264=
XM_011537476.1:c.630G>A	XP_011535778.1:p.Val210=
XM_011537477.1:c.939G>A	XP_011535779.1:p.Val313=
XM_006719963.3:c.774G>A	XP_006720026.2:p.Val258=
XM_011537474.2:c.1023G>A	XP_011535776.2:p.Val341=
XM_011537475.2:c.837G>A	XP_011535777.2:p.Val279=
XM_011537476.2:c.630G>A	XP_011535778.1:p.Val210=
NM_019616.4:c.870G>A MANE Select	NP_062562.1:p.Val290=
NR_051961.2:n.954G>A
NM_001267554.2:c.684G>A	NP_001254483.1:p.Val228=