Canonical Allele Identifier: CA421733993
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169524551G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555313G>A , CM000663.2:g.169555313G>A GRCh38
NC_000001.10:g.169524551G>A , CM000663.1:g.169524551G>A GRCh37
NC_000001.9:g.167791175G>A NCBI36
NG_011806.1:g.36219C>T , LRG_553:g.36219C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.987C>T MANE Select ENSP00000356771.3:p.Cys329=
ENST00000367796.3:c.987C>T ENSP00000356770.3:p.Cys329=
ENST00000367797.7:c.987C>T ENSP00000356771.3:p.Cys329=
NM_000130.4:c.987C>T , LRG_553t1:c.987C>T NP_000121.2:p.Cys329=
XM_017000660.2:c.576C>T XP_016856149.1:p.Cys192=
NM_000130.5:c.987C>T MANE Select NP_000121.2:p.Cys329=