Canonical Allele Identifier: CA343132166
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555308T>C , CM000663.2:g.169555308T>C GRCh38
NC_000001.10:g.169524546T>C , CM000663.1:g.169524546T>C GRCh37
NC_000001.9:g.167791170T>C NCBI36
NG_011806.1:g.36224A>G , LRG_553:g.36224A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.992A>G MANE Select ENSP00000356771.3:p.Lys331Arg
ENST00000367796.3:c.992A>G ENSP00000356770.3:p.Lys331Arg
ENST00000367797.7:c.992A>G ENSP00000356771.3:p.Lys331Arg
NM_000130.4:c.992A>G , LRG_553t1:c.992A>G NP_000121.2:p.Lys331Arg
XM_017000660.2:c.581A>G XP_016856149.1:p.Lys194Arg
NM_000130.5:c.992A>G MANE Select NP_000121.2:p.Lys331Arg