Canonical Allele Identifier: CA343130643

Gene: F5

Linked Data

• dbSNP Id: rs1659547011
• MyVariant Identifiers: chr1:g.169498981T>C (hg19) ; chr1:g.169529743T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529743T>C , CM000663.2:g.169529743T>C	GRCh38
NC_000001.10:g.169498981T>C , CM000663.1:g.169498981T>C	GRCh37
NC_000001.9:g.167765605T>C	NCBI36
NG_011806.1:g.61789A>G , LRG_553:g.61789A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5284A>G MANE Select	ENSP00000356771.3:p.Met1762Val
ENST00000367796.3:c.5299A>G	ENSP00000356770.3:p.Met1767Val
ENST00000367797.7:c.5284A>G	ENSP00000356771.3:p.Met1762Val
NM_000130.4:c.5284A>G , LRG_553t1:c.5284A>G	NP_000121.2:p.Met1762Val
XM_017000660.2:c.4873A>G	XP_016856149.1:p.Met1625Val
NM_000130.5:c.5284A>G MANE Select	NP_000121.2:p.Met1762Val