Canonical Allele Identifier: CA343124897
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169495192A>T (hg19) chr1:g.169525954A>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5663T>A MANE Select ENSP00000356771.3:p.Val1888Asp
ENST00000367796.3:c.5678T>A ENSP00000356770.3:p.Val1893Asp
ENST00000367797.7:c.5663T>A ENSP00000356771.3:p.Val1888Asp
NM_000130.4:c.5663T>A , LRG_553t1:c.5663T>A NP_000121.2:p.Val1888Asp
XM_017000660.2:c.5252T>A XP_016856149.1:p.Val1751Asp
NM_000130.5:c.5663T>A MANE Select NP_000121.2:p.Val1888Asp
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