Canonical Allele Identifier: CA485423856

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772806C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118492C>G , CM000675.2:g.113118492C>G	GRCh38
NC_000013.10:g.113772806C>G , CM000675.1:g.113772806C>G	GRCh37
NC_000013.9:g.112820807C>G	NCBI36
NG_009258.1:g.694C>G , LRG_548:g.694C>G
NG_009262.1:g.17702C>G , LRG_554:g.17702C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.819C>G MANE Select	ENSP00000329546.4:p.Val273=
ENST00000346342.7:c.819C>G	ENSP00000329546.3:p.Val273=
ENST00000375581.3:c.885C>G	ENSP00000364731.3:p.Val295=
ENST00000541084.5:c.633C>G	ENSP00000442051.2:p.Val211=
NM_000131.4:c.885C>G , LRG_554t1:c.885C>G	NP_000122.1:p.Val295=
NM_001267554.1:c.633C>G	NP_001254483.1:p.Val211=
NM_019616.3:c.819C>G , LRG_554t2:c.819C>G	NP_062562.1:p.Val273=
NR_051961.1:n.906C>G
XM_006719963.2:c.678C>G	XP_006720026.1:p.Val226=
XM_011537474.1:c.927C>G	XP_011535776.1:p.Val309=
XM_011537475.1:c.741C>G	XP_011535777.1:p.Val247=
XM_011537476.1:c.579C>G	XP_011535778.1:p.Val193=
XM_011537477.1:c.888C>G	XP_011535779.1:p.Val296=
XM_006719963.3:c.723C>G	XP_006720026.2:p.Val241=
XM_011537474.2:c.972C>G	XP_011535776.2:p.Val324=
XM_011537475.2:c.786C>G	XP_011535777.2:p.Val262=
XM_011537476.2:c.579C>G	XP_011535778.1:p.Val193=
NM_019616.4:c.819C>G MANE Select	NP_062562.1:p.Val273=
NR_051961.2:n.903C>G
NM_001267554.2:c.633C>G	NP_001254483.1:p.Val211=