Canonical Allele Identifier: CA414913702
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154156912A>C (hg19) chrX:g.154928637A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928637A>C , CM000685.2:g.154928637A>C GRCh38
NC_000023.10:g.154156912A>C , CM000685.1:g.154156912A>C GRCh37
NC_000023.9:g.153810106A>C NCBI36
NG_011403.1:g.99087T>G
NG_011403.2:g.99087T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5153T>G MANE Select ENSP00000353393.4:p.Phe1718Cys
ENST00000360256.8:c.5153T>G ENSP00000353393.4:p.Phe1718Cys
NM_000132.3:c.5153T>G NP_000123.1:p.Phe1718Cys
XM_011531126.1:c.5048T>G XP_011529428.1:p.Phe1683Cys
NM_000132.4:c.5153T>G MANE Select NP_000123.1:p.Phe1718Cys
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