Canonical Allele Identifier: CA343124893

Gene: F5

Linked Data

• dbSNP Id: rs1571562780
• MyVariant Identifiers: chr1:g.169495192A>C (hg19) ; chr1:g.169525954A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169525954A>C , CM000663.2:g.169525954A>C	GRCh38
NC_000001.10:g.169495192A>C , CM000663.1:g.169495192A>C	GRCh37
NC_000001.9:g.167761816A>C	NCBI36
NG_011806.1:g.65578T>G , LRG_553:g.65578T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5663T>G MANE Select	ENSP00000356771.3:p.Val1888Gly
ENST00000367796.3:c.5678T>G	ENSP00000356770.3:p.Val1893Gly
ENST00000367797.7:c.5663T>G	ENSP00000356771.3:p.Val1888Gly
NM_000130.4:c.5663T>G , LRG_553t1:c.5663T>G	NP_000121.2:p.Val1888Gly
XM_017000660.2:c.5252T>G	XP_016856149.1:p.Val1751Gly
NM_000130.5:c.5663T>G MANE Select	NP_000121.2:p.Val1888Gly