Canonical Allele Identifier: CA10567992
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs782484860
ExAC: X:154133322 A / T
gnomAD v2: X-154133322-A-T
gnomAD v4: X-154905047-A-T
MyVariant Identifiers: chrX:g.154133322A>T (hg19) chrX:g.154905047A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154905047A>T , CM000685.2:g.154905047A>T GRCh38
NC_000023.10:g.154133322A>T , CM000685.1:g.154133322A>T GRCh37
NC_000023.9:g.153786516A>T NCBI36
NG_011403.1:g.122677T>A
NG_011403.2:g.122677T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5374-24T>A MANE Select ENSP00000353393.4:n.5374-24T>A
ENST00000360256.8:c.5374-24T>A ENSP00000353393.4:n.5374-24T>A
NM_000132.3:c.5374-24T>A NP_000123.1:n.5374-24T>A
XM_011531126.1:c.5269-24T>A XP_011529428.1:n.5269-24T>A
NM_000132.4:c.5374-24T>A MANE Select NP_000123.1:n.5374-24T>A
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