Canonical Allele Identifier: CA343130951
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555203A>T , CM000663.2:g.169555203A>T GRCh38
NC_000001.10:g.169524441A>T , CM000663.1:g.169524441A>T GRCh37
NC_000001.9:g.167791065A>T NCBI36
NG_011806.1:g.36329T>A , LRG_553:g.36329T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.1097T>A MANE Select ENSP00000356771.3:p.Val366Glu
ENST00000367796.3:c.1097T>A ENSP00000356770.3:p.Val366Glu
ENST00000367797.7:c.1097T>A ENSP00000356771.3:p.Val366Glu
NM_000130.4:c.1097T>A , LRG_553t1:c.1097T>A NP_000121.2:p.Val366Glu
XM_017000660.2:c.686T>A XP_016856149.1:p.Val229Glu
NM_000130.5:c.1097T>A MANE Select NP_000121.2:p.Val366Glu