Canonical Allele Identifier: CA343142077
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572286T>A , CM000663.2:g.169572286T>A GRCh38
NC_000001.10:g.169541524T>A , CM000663.1:g.169541524T>A GRCh37
NC_000001.9:g.167808148T>A NCBI36
NG_011806.1:g.19246A>T , LRG_553:g.19246A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.308A>T MANE Select ENSP00000356771.3:p.Lys103Ile
ENST00000367796.3:c.308A>T ENSP00000356770.3:p.Lys103Ile
ENST00000367797.7:c.308A>T ENSP00000356771.3:p.Lys103Ile
NM_000130.4:c.308A>T , LRG_553t1:c.308A>T NP_000121.2:p.Lys103Ile
XM_017000660.2:c.-104A>T XP_016856149.1:n.-104A>T
NM_000130.5:c.308A>T MANE Select NP_000121.2:p.Lys103Ile