Canonical Allele Identifier: CA2695152869
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154902044-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902045del , CM000685.2:g.154902045del GRCh38
NC_000023.10:g.154130320del , CM000685.1:g.154130320del GRCh37
NC_000023.9:g.153783514del NCBI36
NG_011403.1:g.125679del
NG_011403.2:g.125679del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6115+6del MANE Select ENSP00000353393.4:n.6115+6del
ENST00000360256.8:c.6115+6del ENSP00000353393.4:n.6115+6del
NM_000132.3:c.6115+6del NP_000123.1:n.6115+6del
XM_011531126.1:c.6010+6del XP_011529428.1:n.6010+6del
NM_000132.4:c.6115+6del MANE Select NP_000123.1:n.6115+6del
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