Canonical Allele Identifier: CA2555536999
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928458del , CM000685.2:g.154928458del GRCh38
NC_000023.10:g.154156733del , CM000685.1:g.154156733del GRCh37
NC_000023.9:g.153809927del NCBI36
NG_011403.1:g.99267del
NG_011403.2:g.99267del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5219+114del MANE Select ENSP00000353393.4:n.5219+114del
ENST00000360256.8:c.5219+114del ENSP00000353393.4:n.5219+114del
NM_000132.3:c.5219+114del NP_000123.1:n.5219+114del
XM_011531126.1:c.5114+114del XP_011529428.1:n.5114+114del
NM_000132.4:c.5219+114del MANE Select NP_000123.1:n.5219+114del
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