Canonical Allele Identifier: CA388785955

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772823A>G (hg19) ; chr13:g.113118509A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118509A>G , CM000675.2:g.113118509A>G	GRCh38
NC_000013.10:g.113772823A>G , CM000675.1:g.113772823A>G	GRCh37
NC_000013.9:g.112820824A>G	NCBI36
NG_009258.1:g.711A>G , LRG_548:g.711A>G
NG_009262.1:g.17719A>G , LRG_554:g.17719A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.836A>G MANE Select	ENSP00000329546.4:p.His279Arg
ENST00000346342.7:c.836A>G	ENSP00000329546.3:p.His279Arg
ENST00000375581.3:c.902A>G	ENSP00000364731.3:p.His301Arg
ENST00000541084.5:c.650A>G	ENSP00000442051.2:p.His217Arg
NM_000131.4:c.902A>G , LRG_554t1:c.902A>G	NP_000122.1:p.His301Arg
NM_001267554.1:c.650A>G	NP_001254483.1:p.His217Arg
NM_019616.3:c.836A>G , LRG_554t2:c.836A>G	NP_062562.1:p.His279Arg
NR_051961.1:n.923A>G
XM_006719963.2:c.695A>G	XP_006720026.1:p.His232Arg
XM_011537474.1:c.944A>G	XP_011535776.1:p.His315Arg
XM_011537475.1:c.758A>G	XP_011535777.1:p.His253Arg
XM_011537476.1:c.596A>G	XP_011535778.1:p.His199Arg
XM_011537477.1:c.905A>G	XP_011535779.1:p.His302Arg
XM_006719963.3:c.740A>G	XP_006720026.2:p.His247Arg
XM_011537474.2:c.989A>G	XP_011535776.2:p.His330Arg
XM_011537475.2:c.803A>G	XP_011535777.2:p.His268Arg
XM_011537476.2:c.596A>G	XP_011535778.1:p.His199Arg
NM_019616.4:c.836A>G MANE Select	NP_062562.1:p.His279Arg
NR_051961.2:n.920A>G
NM_001267554.2:c.650A>G	NP_001254483.1:p.His217Arg