Canonical Allele Identifier: CA343125172

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169495228G>C (hg19) ; chr1:g.169525990G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169525990G>C , CM000663.2:g.169525990G>C	GRCh38
NC_000001.10:g.169495228G>C , CM000663.1:g.169495228G>C	GRCh37
NC_000001.9:g.167761852G>C	NCBI36
NG_011806.1:g.65542C>G , LRG_553:g.65542C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5627C>G MANE Select	ENSP00000356771.3:p.Ala1876Gly
ENST00000367796.3:c.5642C>G	ENSP00000356770.3:p.Ala1881Gly
ENST00000367797.7:c.5627C>G	ENSP00000356771.3:p.Ala1876Gly
NM_000130.4:c.5627C>G , LRG_553t1:c.5627C>G	NP_000121.2:p.Ala1876Gly
XM_017000660.2:c.5216C>G	XP_016856149.1:p.Ala1739Gly
NM_000130.5:c.5627C>G MANE Select	NP_000121.2:p.Ala1876Gly