Canonical Allele Identifier: CA421735125
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169495197T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169525959T>C , CM000663.2:g.169525959T>C GRCh38
NC_000001.10:g.169495197T>C , CM000663.1:g.169495197T>C GRCh37
NC_000001.9:g.167761821T>C NCBI36
NG_011806.1:g.65573A>G , LRG_553:g.65573A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5658A>G MANE Select ENSP00000356771.3:p.Thr1886=
ENST00000367796.3:c.5673A>G ENSP00000356770.3:p.Thr1891=
ENST00000367797.7:c.5658A>G ENSP00000356771.3:p.Thr1886=
NM_000130.4:c.5658A>G , LRG_553t1:c.5658A>G NP_000121.2:p.Thr1886=
XM_017000660.2:c.5247A>G XP_016856149.1:p.Thr1749=
NM_000130.5:c.5658A>G MANE Select NP_000121.2:p.Thr1886=
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