Canonical Allele Identifier: CA343132086
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555302G>T , CM000663.2:g.169555302G>T GRCh38
NC_000001.10:g.169524540G>T , CM000663.1:g.169524540G>T GRCh37
NC_000001.9:g.167791164G>T NCBI36
NG_011806.1:g.36230C>A , LRG_553:g.36230C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.998C>A MANE Select ENSP00000356771.3:p.Thr333Asn
ENST00000367796.3:c.998C>A ENSP00000356770.3:p.Thr333Asn
ENST00000367797.7:c.998C>A ENSP00000356771.3:p.Thr333Asn
NM_000130.4:c.998C>A , LRG_553t1:c.998C>A NP_000121.2:p.Thr333Asn
XM_017000660.2:c.587C>A XP_016856149.1:p.Thr196Asn
NM_000130.5:c.998C>A MANE Select NP_000121.2:p.Thr333Asn