Canonical Allele Identifier: CA343128698
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552663G>C , CM000663.2:g.169552663G>C GRCh38
NC_000001.10:g.169521901G>C , CM000663.1:g.169521901G>C GRCh37
NC_000001.9:g.167788525G>C NCBI36
NG_011806.1:g.38869C>G , LRG_553:g.38869C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1190C>G MANE Select ENSP00000356771.3:p.Thr397Arg
ENST00000367796.3:c.1190C>G ENSP00000356770.3:p.Thr397Arg
ENST00000367797.7:c.1190C>G ENSP00000356771.3:p.Thr397Arg
NM_000130.4:c.1190C>G , LRG_553t1:c.1190C>G NP_000121.2:p.Thr397Arg
XM_017000660.2:c.779C>G XP_016856149.1:p.Thr260Arg
NM_000130.5:c.1190C>G MANE Select NP_000121.2:p.Thr397Arg