Canonical Allele Identifier: CA343124931
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169495196C>T (hg19) chr1:g.169525958C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169525958C>T , CM000663.2:g.169525958C>T GRCh38
NC_000001.10:g.169495196C>T , CM000663.1:g.169495196C>T GRCh37
NC_000001.9:g.167761820C>T NCBI36
NG_011806.1:g.65574G>A , LRG_553:g.65574G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5659G>A MANE Select ENSP00000356771.3:p.Glu1887Lys
ENST00000367796.3:c.5674G>A ENSP00000356770.3:p.Glu1892Lys
ENST00000367797.7:c.5659G>A ENSP00000356771.3:p.Glu1887Lys
NM_000130.4:c.5659G>A , LRG_553t1:c.5659G>A NP_000121.2:p.Glu1887Lys
XM_017000660.2:c.5248G>A XP_016856149.1:p.Glu1750Lys
NM_000130.5:c.5659G>A MANE Select NP_000121.2:p.Glu1887Lys
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