Canonical Allele Identifier: CA414917953
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154197704G>T (hg19) chrX:g.154969429G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969429G>T , CM000685.2:g.154969429G>T GRCh38
NC_000023.10:g.154197704G>T , CM000685.1:g.154197704G>T GRCh37
NC_000023.9:g.153850898G>T NCBI36
NG_011403.1:g.58295C>A
NG_011403.2:g.58295C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.911C>A MANE Select ENSP00000353393.4:p.Ser304Tyr
ENST00000647125.1:c.*787C>A ENSP00000496062.1:n.*787C>A
ENST00000360256.8:c.911C>A ENSP00000353393.4:p.Ser304Tyr
NM_000132.3:c.911C>A NP_000123.1:p.Ser304Tyr
XM_011531126.1:c.806C>A XP_011529428.1:p.Ser269Tyr
NM_000132.4:c.911C>A MANE Select NP_000123.1:p.Ser304Tyr
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