Canonical Allele Identifier: CA421930075
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169510254A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541016A>T , CM000663.2:g.169541016A>T GRCh38
NC_000001.10:g.169510254A>T , CM000663.1:g.169510254A>T GRCh37
NC_000001.9:g.167776878A>T NCBI36
NG_011806.1:g.50516T>A , LRG_553:g.50516T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.4074T>A MANE Select ENSP00000356771.3:p.Ser1358=
ENST00000367796.3:c.4089T>A ENSP00000356770.3:p.Ser1363=
ENST00000367797.7:c.4074T>A ENSP00000356771.3:p.Ser1358=
NM_000130.4:c.4074T>A , LRG_553t1:c.4074T>A NP_000121.2:p.Ser1358=
XM_017000660.2:c.3663T>A XP_016856149.1:p.Ser1221=
NM_000130.5:c.4074T>A MANE Select NP_000121.2:p.Ser1358=