Canonical Allele Identifier: CA343142038

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169541513C>A (hg19) ; chr1:g.169572275C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572275C>A , CM000663.2:g.169572275C>A	GRCh38
NC_000001.10:g.169541513C>A , CM000663.1:g.169541513C>A	GRCh37
NC_000001.9:g.167808137C>A	NCBI36
NG_011806.1:g.19257G>T , LRG_553:g.19257G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.319G>T MANE Select	ENSP00000356771.3:p.Asp107Tyr
ENST00000367796.3:c.319G>T	ENSP00000356770.3:p.Asp107Tyr
ENST00000367797.7:c.319G>T	ENSP00000356771.3:p.Asp107Tyr
NM_000130.4:c.319G>T , LRG_553t1:c.319G>T	NP_000121.2:p.Asp107Tyr
XM_017000660.2:c.-93G>T	XP_016856149.1:n.-93G>T
NM_000130.5:c.319G>T MANE Select	NP_000121.2:p.Asp107Tyr