Canonical Allele Identifier: CA2695152819
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154901937-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154901939del , CM000685.2:g.154901939del GRCh38
NC_000023.10:g.154130214del , CM000685.1:g.154130214del GRCh37
NC_000023.9:g.153783408del NCBI36
NG_011403.1:g.125786del
NG_011403.2:g.125786del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6115+113del MANE Select ENSP00000353393.4:n.6115+113del
ENST00000360256.8:c.6115+113del ENSP00000353393.4:n.6115+113del
NM_000132.3:c.6115+113del NP_000123.1:n.6115+113del
XM_011531126.1:c.6010+113del XP_011529428.1:n.6010+113del
NM_000132.4:c.6115+113del MANE Select NP_000123.1:n.6115+113del
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