Canonical Allele Identifier: CA519357695
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154133281C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154905006C>T , CM000685.2:g.154905006C>T GRCh38
NC_000023.10:g.154133281C>T , CM000685.1:g.154133281C>T GRCh37
NC_000023.9:g.153786475C>T NCBI36
NG_011403.1:g.122718G>A
NG_011403.2:g.122718G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5391G>A MANE Select ENSP00000353393.4:p.Gln1797=
ENST00000360256.8:c.5391G>A ENSP00000353393.4:p.Gln1797=
NM_000132.3:c.5391G>A NP_000123.1:p.Gln1797=
XM_011531126.1:c.5286G>A XP_011529428.1:p.Gln1762=
NM_000132.4:c.5391G>A MANE Select NP_000123.1:p.Gln1797=
Search 100 bp 5'
Search 100 bp 3'