Canonical Allele Identifier: CA2695168094
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154904638-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904640del , CM000685.2:g.154904640del GRCh38
NC_000023.10:g.154132915del , CM000685.1:g.154132915del GRCh37
NC_000023.9:g.153786109del NCBI36
NG_011403.1:g.123085del
NG_011403.2:g.123085del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5587-115del MANE Select ENSP00000353393.4:n.5587-115del
ENST00000360256.8:c.5587-115del ENSP00000353393.4:n.5587-115del
NM_000132.3:c.5587-115del NP_000123.1:n.5587-115del
XM_011531126.1:c.5482-115del XP_011529428.1:n.5482-115del
NM_000132.4:c.5587-115del MANE Select NP_000123.1:n.5587-115del
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