Canonical Allele Identifier: CA10633924
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 311255
ClinVar RCV Id: RCV000327609
dbSNP Id: rs3093254

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113119999G>A , CM000675.2:g.113119999G>A GRCh38
NC_000013.10:g.113774313G>A , CM000675.1:g.113774313G>A GRCh37
NC_000013.9:g.112822314G>A NCBI36
NG_009258.1:g.2201G>A , LRG_548:g.2201G>A
NG_009262.1:g.19209G>A , LRG_554:g.19209G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000346342.8:c.*991G>A MANE Select ENSP00000329546.4:p.=
ENST00000346342.7:c.*991G>A ENSP00000329546.3:p.=
ENST00000375581.3:c.*991G>A ENSP00000364731.3:p.=
ENST00000541084.5:c.*991G>A ENSP00000442051.2:p.=
NM_000131.4:c.*991G>A , LRG_554t1:c.*991G>A NP_000122.1:p.=
NM_001267554.1:c.*991G>A NP_001254483.1:p.=
NM_019616.3:c.*991G>A , LRG_554t2:c.*991G>A NP_062562.1:p.=
NR_051961.1:n.2413G>A
XM_006719963.2:c.*991G>A XP_006720026.1:p.=
XM_011537474.1:c.*991G>A XP_011535776.1:p.=
XM_011537475.1:c.*991G>A XP_011535777.1:p.=
XM_011537476.1:c.*991G>A XP_011535778.1:p.=
XM_011537477.1:c.*991G>A XP_011535779.1:p.=
XM_006719963.3:c.*991G>A XP_006720026.2:p.=
XM_011537474.2:c.*991G>A XP_011535776.2:p.=
XM_011537475.2:c.*991G>A XP_011535777.2:p.=
XM_011537476.2:c.*991G>A XP_011535778.1:p.=
NM_019616.4:c.*991G>A MANE Select NP_062562.1:p.=
NR_051961.2:n.2410G>A
NM_001267554.2:c.*991G>A NP_001254483.1:p.=