Canonical Allele Identifier: CA2695153029
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154903949-TCGTACAGTGA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903950_154903959del , CM000685.2:g.154903950_154903959del GRCh38
NC_000023.10:g.154132225_154132234del , CM000685.1:g.154132225_154132234del GRCh37
NC_000023.9:g.153785419_153785428del NCBI36
NG_011403.1:g.123765_123774del
NG_011403.2:g.123765_123774del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5945_5954del MANE Select ENSP00000353393.4:p.Phe1982Ter
ENST00000360256.8:c.5945_5954del ENSP00000353393.4:p.Phe1982Ter
NM_000132.3:c.5945_5954del NP_000123.1:p.Phe1982Ter
XM_011531126.1:c.5840_5849del XP_011529428.1:p.Phe1947Ter
NM_000132.4:c.5945_5954del MANE Select NP_000123.1:p.Phe1982Ter
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