Canonical Allele Identifier: CA2695237950
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928799del , CM000685.2:g.154928799del GRCh38
NC_000023.10:g.154157074del , CM000685.1:g.154157074del GRCh37
NC_000023.9:g.153810268del NCBI36
NG_011403.1:g.98925del
NG_011403.2:g.98925del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4991del MANE Select ENSP00000353393.4:p.Arg1664ProfsTer6
ENST00000360256.8:c.4991del ENSP00000353393.4:p.Arg1664ProfsTer6
NM_000132.3:c.4991del NP_000123.1:p.Arg1664ProfsTer6
XM_011531126.1:c.4886del XP_011529428.1:p.Arg1629ProfsTer6
NM_000132.4:c.4991del MANE Select NP_000123.1:p.Arg1664ProfsTer6
Search 100 bp 5'
Search 100 bp 3'