Canonical Allele Identifier: CA7060164
Gene: F7 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs121964931

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113118518C>T , CM000675.2:g.113118518C>T GRCh38
NC_000013.10:g.113772832C>T , CM000675.1:g.113772832C>T GRCh37
NC_000013.9:g.112820833C>T NCBI36
NG_009258.1:g.720C>T , LRG_548:g.720C>T
NG_009262.1:g.17728C>T , LRG_554:g.17728C>T

Transcript Alleles

HGVS Amino-acid change
NM_000131.4:c.911C>T , LRG_554t1:c.911C>T NP_000122.1:p.Ala304Val
NM_001267554.1:c.659C>T VV NP_001254483.1:p.Ala220Val
NM_019616.3:c.845C>T , LRG_554t2:c.845C>T NP_062562.1:p.Ala282Val
NR_051961.1:n.932C>T
XM_006719963.2:c.704C>T XP_006720026.1:p.Ala235Val
XM_011537474.1:c.953C>T XP_011535776.1:p.Ala318Val
XM_011537475.1:c.767C>T XP_011535777.1:p.Ala256Val
XM_011537476.1:c.605C>T XP_011535778.1:p.Ala202Val
XM_011537477.1:c.914C>T XP_011535779.1:p.Ala305Val
XM_006719963.3:c.749C>T XP_006720026.2:p.Ala250Val
XM_011537474.2:c.998C>T XP_011535776.2:p.Ala333Val
XM_011537475.2:c.812C>T XP_011535777.2:p.Ala271Val
XM_011537476.2:c.605C>T XP_011535778.1:p.Ala202Val
ENST00000346342.7:c.845C>T ENSP00000329546.3:p.Ala282Val
ENST00000375581.3:c.911C>T ENSP00000364731.3:p.Ala304Val
ENST00000541084.5:c.659C>T ENSP00000442051.2:p.Ala220Val