Canonical Allele Identifier: CA343131249

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169499038C>T (hg19) ; chr1:g.169529800C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529800C>T , CM000663.2:g.169529800C>T	GRCh38
NC_000001.10:g.169499038C>T , CM000663.1:g.169499038C>T	GRCh37
NC_000001.9:g.167765662C>T	NCBI36
NG_011806.1:g.61732G>A , LRG_553:g.61732G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5227G>A MANE Select	ENSP00000356771.3:p.Gly1743Ser
ENST00000367796.3:c.5242G>A	ENSP00000356770.3:p.Gly1748Ser
ENST00000367797.7:c.5227G>A	ENSP00000356771.3:p.Gly1743Ser
NM_000130.4:c.5227G>A , LRG_553t1:c.5227G>A	NP_000121.2:p.Gly1743Ser
XM_017000660.2:c.4816G>A	XP_016856149.1:p.Gly1606Ser
NM_000130.5:c.5227G>A MANE Select	NP_000121.2:p.Gly1743Ser