Canonical Allele Identifier: CA343142007
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572266A>T , CM000663.2:g.169572266A>T GRCh38
NC_000001.10:g.169541504A>T , CM000663.1:g.169541504A>T GRCh37
NC_000001.9:g.167808128A>T NCBI36
NG_011806.1:g.19266T>A , LRG_553:g.19266T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.328T>A MANE Select ENSP00000356771.3:p.Leu110Met
ENST00000367796.3:c.328T>A ENSP00000356770.3:p.Leu110Met
ENST00000367797.7:c.328T>A ENSP00000356771.3:p.Leu110Met
NM_000130.4:c.328T>A , LRG_553t1:c.328T>A NP_000121.2:p.Leu110Met
XM_017000660.2:c.-84T>A XP_016856149.1:n.-84T>A
NM_000130.5:c.328T>A MANE Select NP_000121.2:p.Leu110Met