Canonical Allele Identifier: CA2695170503
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-155022649-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022652del , CM000685.2:g.155022652del GRCh38
NC_000023.10:g.154250927del , CM000685.1:g.154250927del GRCh37
NC_000023.9:g.153904121del NCBI36
NG_011403.1:g.5074del
NG_011403.2:g.5074del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.-98del MANE Select ENSP00000353393.4:n.-98del
ENST00000647125.1:c.-98del ENSP00000496062.1:n.-98del
ENST00000360256.8:c.-98del ENSP00000353393.4:n.-98del
ENST00000423959.5:c.38+4130del ENSP00000409446.1:n.38+4130del
ENST00000453950.1:c.39-154del ENSP00000389153.1:n.39-154del
NM_000132.3:c.-98del NP_000123.1:n.-98del
XM_011531126.1:c.38+4130del XP_011529428.1:n.38+4130del
NM_000132.4:c.-98del MANE Select NP_000123.1:n.-98del
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