Canonical Allele Identifier: CA519372655
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154221320A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154993045A>G , CM000685.2:g.154993045A>G GRCh38
NC_000023.10:g.154221320A>G , CM000685.1:g.154221320A>G GRCh37
NC_000023.9:g.153874514A>G NCBI36
NG_011403.1:g.34679T>C
NG_011403.2:g.34679T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.492T>C MANE Select ENSP00000353393.4:p.Gly164=
ENST00000647125.1:c.*278T>C ENSP00000496062.1:n.*278T>C
ENST00000360256.8:c.492T>C ENSP00000353393.4:p.Gly164=
ENST00000423959.5:c.387T>C ENSP00000409446.1:p.Gly129=
ENST00000453950.1:c.474T>C ENSP00000389153.1:p.Gly158=
NM_000132.3:c.492T>C NP_000123.1:p.Gly164=
XM_011531126.1:c.387T>C XP_011529428.1:p.Gly129=
NM_000132.4:c.492T>C MANE Select NP_000123.1:p.Gly164=
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