Canonical Allele Identifier: CA421737928

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169499015G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529777G>A , CM000663.2:g.169529777G>A	GRCh38
NC_000001.10:g.169499015G>A , CM000663.1:g.169499015G>A	GRCh37
NC_000001.9:g.167765639G>A	NCBI36
NG_011806.1:g.61755C>T , LRG_553:g.61755C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5250C>T MANE Select	ENSP00000356771.3:p.Ile1750=
ENST00000367796.3:c.5265C>T	ENSP00000356770.3:p.Ile1755=
ENST00000367797.7:c.5250C>T	ENSP00000356771.3:p.Ile1750=
NM_000130.4:c.5250C>T , LRG_553t1:c.5250C>T	NP_000121.2:p.Ile1750=
XM_017000660.2:c.4839C>T	XP_016856149.1:p.Ile1613=
NM_000130.5:c.5250C>T MANE Select	NP_000121.2:p.Ile1750=