Canonical Allele Identifier: CA343128673

Gene: F5

Linked Data

• dbSNP Id: rs756074656
• MyVariant Identifiers: chr1:g.169521896A>T (hg19) ; chr1:g.169552658A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552658A>T , CM000663.2:g.169552658A>T	GRCh38
NC_000001.10:g.169521896A>T , CM000663.1:g.169521896A>T	GRCh37
NC_000001.9:g.167788520A>T	NCBI36
NG_011806.1:g.38874T>A , LRG_553:g.38874T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1195T>A MANE Select	ENSP00000356771.3:p.Tyr399Asn
ENST00000367796.3:c.1195T>A	ENSP00000356770.3:p.Tyr399Asn
ENST00000367797.7:c.1195T>A	ENSP00000356771.3:p.Tyr399Asn
NM_000130.4:c.1195T>A , LRG_553t1:c.1195T>A	NP_000121.2:p.Tyr399Asn
XM_017000660.2:c.784T>A	XP_016856149.1:p.Tyr262Asn
NM_000130.5:c.1195T>A MANE Select	NP_000121.2:p.Tyr399Asn