Canonical Allele Identifier: CA2695152072
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154896282-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896283del , CM000685.2:g.154896283del GRCh38
NC_000023.10:g.154124558del , CM000685.1:g.154124558del GRCh37
NC_000023.9:g.153777752del NCBI36
NG_011403.1:g.131441del
NG_011403.2:g.131441del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6274-51del MANE Select ENSP00000353393.4:n.6274-51del
ENST00000360256.8:c.6274-51del ENSP00000353393.4:n.6274-51del
NM_000132.3:c.6274-51del NP_000123.1:n.6274-51del
XM_011531126.1:c.6169-51del XP_011529428.1:n.6169-51del
NM_000132.4:c.6274-51del MANE Select NP_000123.1:n.6274-51del
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