Canonical Allele Identifier: CA343130940
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555201T>G , CM000663.2:g.169555201T>G GRCh38
NC_000001.10:g.169524439T>G , CM000663.1:g.169524439T>G GRCh37
NC_000001.9:g.167791063T>G NCBI36
NG_011806.1:g.36331A>C , LRG_553:g.36331A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.1099A>C MANE Select ENSP00000356771.3:p.Ile367Leu
ENST00000367796.3:c.1099A>C ENSP00000356770.3:p.Ile367Leu
ENST00000367797.7:c.1099A>C ENSP00000356771.3:p.Ile367Leu
NM_000130.4:c.1099A>C , LRG_553t1:c.1099A>C NP_000121.2:p.Ile367Leu
XM_017000660.2:c.688A>C XP_016856149.1:p.Ile230Leu
NM_000130.5:c.1099A>C MANE Select NP_000121.2:p.Ile367Leu