Canonical Allele Identifier: CA2466835810
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073174302
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928799_154928800dup , CM000685.2:g.154928799_154928800dup GRCh38
NC_000023.10:g.154157074_154157075dup , CM000685.1:g.154157074_154157075dup GRCh37
NC_000023.9:g.153810268_153810269dup NCBI36
NG_011403.1:g.98925_98926dup
NG_011403.2:g.98925_98926dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4991_4992dup MANE Select ENSP00000353393.4:p.His1665AlafsTer6
ENST00000360256.8:c.4991_4992dup ENSP00000353393.4:p.His1665AlafsTer6
NM_000132.3:c.4991_4992dup NP_000123.1:p.His1665AlafsTer6
XM_011531126.1:c.4886_4887dup XP_011529428.1:p.His1630AlafsTer6
NM_000132.4:c.4991_4992dup MANE Select NP_000123.1:p.His1665AlafsTer6
Search 100 bp 5'
Search 100 bp 3'