Canonical Allele Identifier: CA414901745
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154931373-G-T
MyVariant Identifiers: chrX:g.154159648G>T (hg19) chrX:g.154931373G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154931373G>T , CM000685.2:g.154931373G>T GRCh38
NC_000023.10:g.154159648G>T , CM000685.1:g.154159648G>T GRCh37
NC_000023.9:g.153812842G>T NCBI36
NG_011403.1:g.96351C>A
NG_011403.2:g.96351C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.2417C>A MANE Select ENSP00000353393.4:p.Ser806Tyr
ENST00000647125.1:c.*2083C>A ENSP00000496062.1:n.*2083C>A
ENST00000360256.8:c.2417C>A ENSP00000353393.4:p.Ser806Tyr
NM_000132.3:c.2417C>A NP_000123.1:p.Ser806Tyr
XM_011531126.1:c.2312C>A XP_011529428.1:p.Ser771Tyr
NM_000132.4:c.2417C>A MANE Select NP_000123.1:p.Ser806Tyr
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