Canonical Allele Identifier: CA421930431

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169510902T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541664T>C , CM000663.2:g.169541664T>C	GRCh38
NC_000001.10:g.169510902T>C , CM000663.1:g.169510902T>C	GRCh37
NC_000001.9:g.167777526T>C	NCBI36
NG_011806.1:g.49868A>G , LRG_553:g.49868A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3426A>G MANE Select	ENSP00000356771.3:p.Ser1142=
ENST00000367796.3:c.3441A>G	ENSP00000356770.3:p.Ser1147=
ENST00000367797.7:c.3426A>G	ENSP00000356771.3:p.Ser1142=
NM_000130.4:c.3426A>G , LRG_553t1:c.3426A>G	NP_000121.2:p.Ser1142=
XM_017000660.2:c.3015A>G	XP_016856149.1:p.Ser1005=
NM_000130.5:c.3426A>G MANE Select	NP_000121.2:p.Ser1142=