Canonical Allele Identifier: CA414919940
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154225282A>C (hg19) chrX:g.154997007A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997007A>C , CM000685.2:g.154997007A>C GRCh38
NC_000023.10:g.154225282A>C , CM000685.1:g.154225282A>C GRCh37
NC_000023.9:g.153878476A>C NCBI36
NG_011403.1:g.30717T>G
NG_011403.2:g.30717T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.354T>G MANE Select ENSP00000353393.4:p.His118Gln
ENST00000647125.1:c.*140T>G ENSP00000496062.1:n.*140T>G
ENST00000360256.8:c.354T>G ENSP00000353393.4:p.His118Gln
ENST00000423959.5:c.249T>G ENSP00000409446.1:p.His83Gln
ENST00000453950.1:c.336T>G ENSP00000389153.1:p.His112Gln
NM_000132.3:c.354T>G NP_000123.1:p.His118Gln
XM_011531126.1:c.249T>G XP_011529428.1:p.His83Gln
NM_000132.4:c.354T>G MANE Select NP_000123.1:p.His118Gln
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