Canonical Allele Identifier: CA2695170435
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-155022299-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022299G>T , CM000685.2:g.155022299G>T GRCh38
NC_000023.10:g.154250574G>T , CM000685.1:g.154250574G>T GRCh37
NC_000023.9:g.153903768G>T NCBI36
NG_011403.1:g.5425C>A
NG_011403.2:g.5425C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.143+111C>A MANE Select ENSP00000353393.4:n.143+111C>A
ENST00000647125.1:c.121+133C>A ENSP00000496062.1:n.121+133C>A
ENST00000360256.8:c.143+111C>A ENSP00000353393.4:n.143+111C>A
ENST00000423959.5:c.38+4481C>A ENSP00000409446.1:n.38+4481C>A
ENST00000453950.1:c.125+111C>A ENSP00000389153.1:n.125+111C>A
NM_000132.3:c.143+111C>A NP_000123.1:n.143+111C>A
XM_011531126.1:c.38+4481C>A XP_011529428.1:n.38+4481C>A
NM_000132.4:c.143+111C>A MANE Select NP_000123.1:n.143+111C>A
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