Canonical Allele Identifier: CA343124884
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169495189C>T (hg19) chr1:g.169525951C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169525951C>T , CM000663.2:g.169525951C>T GRCh38
NC_000001.10:g.169495189C>T , CM000663.1:g.169495189C>T GRCh37
NC_000001.9:g.167761813C>T NCBI36
NG_011806.1:g.65581G>A , LRG_553:g.65581G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5666G>A MANE Select ENSP00000356771.3:p.Gly1889Glu
ENST00000367796.3:c.5681G>A ENSP00000356770.3:p.Gly1894Glu
ENST00000367797.7:c.5666G>A ENSP00000356771.3:p.Gly1889Glu
NM_000130.4:c.5666G>A , LRG_553t1:c.5666G>A NP_000121.2:p.Gly1889Glu
XM_017000660.2:c.5255G>A XP_016856149.1:p.Gly1752Glu
NM_000130.5:c.5666G>A MANE Select NP_000121.2:p.Gly1889Glu
Search 100 bp 5'
Search 100 bp 3'