Canonical Allele Identifier: CA2466828478
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073030810
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154905006dup , CM000685.2:g.154905006dup GRCh38
NC_000023.10:g.154133281dup , CM000685.1:g.154133281dup GRCh37
NC_000023.9:g.153786475dup NCBI36
NG_011403.1:g.122719dup
NG_011403.2:g.122719dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5392dup MANE Select ENSP00000353393.4:p.Ala1798GlyfsTer10
ENST00000360256.8:c.5392dup ENSP00000353393.4:p.Ala1798GlyfsTer10
NM_000132.3:c.5392dup NP_000123.1:p.Ala1798GlyfsTer10
XM_011531126.1:c.5287dup XP_011529428.1:p.Ala1763GlyfsTer10
NM_000132.4:c.5392dup MANE Select NP_000123.1:p.Ala1798GlyfsTer10
Search 100 bp 5'
Search 100 bp 3'