Canonical Allele Identifier: CA2695237869
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902048_154902050del , CM000685.2:g.154902048_154902050del GRCh38
NC_000023.10:g.154130323_154130325del , CM000685.1:g.154130323_154130325del GRCh37
NC_000023.9:g.153783517_153783519del NCBI36
NG_011403.1:g.125674_125676del
NG_011403.2:g.125674_125676del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6115+1_6115+3del MANE Select ENSP00000353393.4:n.6115+1_6115+3del
ENST00000360256.8:c.6115+1_6115+3del ENSP00000353393.4:n.6115+1_6115+3del
NM_000132.3:c.6115+1_6115+3del NP_000123.1:n.6115+1_6115+3del
XM_011531126.1:c.6010+1_6010+3del XP_011529428.1:n.6010+1_6010+3del
NM_000132.4:c.6115+1_6115+3del MANE Select NP_000123.1:n.6115+1_6115+3del
Search 100 bp 5'
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