Canonical Allele Identifier: CA421732521
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169521846T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552608T>C , CM000663.2:g.169552608T>C GRCh38
NC_000001.10:g.169521846T>C , CM000663.1:g.169521846T>C GRCh37
NC_000001.9:g.167788470T>C NCBI36
NG_011806.1:g.38924A>G , LRG_553:g.38924A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1245A>G MANE Select ENSP00000356771.3:p.Glu415=
ENST00000367796.3:c.1245A>G ENSP00000356770.3:p.Glu415=
ENST00000367797.7:c.1245A>G ENSP00000356771.3:p.Glu415=
NM_000130.4:c.1245A>G , LRG_553t1:c.1245A>G NP_000121.2:p.Glu415=
XM_017000660.2:c.834A>G XP_016856149.1:p.Glu278=
NM_000130.5:c.1245A>G MANE Select NP_000121.2:p.Glu415=