Canonical Allele Identifier: CA421733854
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169524512C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555274C>T , CM000663.2:g.169555274C>T GRCh38
NC_000001.10:g.169524512C>T , CM000663.1:g.169524512C>T GRCh37
NC_000001.9:g.167791136C>T NCBI36
NG_011806.1:g.36258G>A , LRG_553:g.36258G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1026G>A MANE Select ENSP00000356771.3:p.Glu342=
ENST00000367796.3:c.1026G>A ENSP00000356770.3:p.Glu342=
ENST00000367797.7:c.1026G>A ENSP00000356771.3:p.Glu342=
NM_000130.4:c.1026G>A , LRG_553t1:c.1026G>A NP_000121.2:p.Glu342=
XM_017000660.2:c.615G>A XP_016856149.1:p.Glu205=
NM_000130.5:c.1026G>A MANE Select NP_000121.2:p.Glu342=