Canonical Allele Identifier: CA343130918
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555200A>G , CM000663.2:g.169555200A>G GRCh38
NC_000001.10:g.169524438A>G , CM000663.1:g.169524438A>G GRCh37
NC_000001.9:g.167791062A>G NCBI36
NG_011806.1:g.36332T>C , LRG_553:g.36332T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.1100T>C MANE Select ENSP00000356771.3:p.Ile367Thr
ENST00000367796.3:c.1100T>C ENSP00000356770.3:p.Ile367Thr
ENST00000367797.7:c.1100T>C ENSP00000356771.3:p.Ile367Thr
NM_000130.4:c.1100T>C , LRG_553t1:c.1100T>C NP_000121.2:p.Ile367Thr
XM_017000660.2:c.689T>C XP_016856149.1:p.Ile230Thr
NM_000130.5:c.1100T>C MANE Select NP_000121.2:p.Ile367Thr