Canonical Allele Identifier: CA421737444

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169498880T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529642T>G , CM000663.2:g.169529642T>G	GRCh38
NC_000001.10:g.169498880T>G , CM000663.1:g.169498880T>G	GRCh37
NC_000001.9:g.167765504T>G	NCBI36
NG_011806.1:g.61890A>C , LRG_553:g.61890A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5385A>C MANE Select	ENSP00000356771.3:p.Thr1795=
ENST00000367796.3:c.5400A>C	ENSP00000356770.3:p.Thr1800=
ENST00000367797.7:c.5385A>C	ENSP00000356771.3:p.Thr1795=
NM_000130.4:c.5385A>C , LRG_553t1:c.5385A>C	NP_000121.2:p.Thr1795=
XM_017000660.2:c.4974A>C	XP_016856149.1:p.Thr1658=
NM_000130.5:c.5385A>C MANE Select	NP_000121.2:p.Thr1795=