Canonical Allele Identifier: CA343132478
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555333A>C , CM000663.2:g.169555333A>C GRCh38
NC_000001.10:g.169524571A>C , CM000663.1:g.169524571A>C GRCh37
NC_000001.9:g.167791195A>C NCBI36
NG_011806.1:g.36199T>G , LRG_553:g.36199T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.967T>G MANE Select ENSP00000356771.3:p.Tyr323Asp
ENST00000367796.3:c.967T>G ENSP00000356770.3:p.Tyr323Asp
ENST00000367797.7:c.967T>G ENSP00000356771.3:p.Tyr323Asp
NM_000130.4:c.967T>G , LRG_553t1:c.967T>G NP_000121.2:p.Tyr323Asp
XM_017000660.2:c.556T>G XP_016856149.1:p.Tyr186Asp
NM_000130.5:c.967T>G MANE Select NP_000121.2:p.Tyr323Asp