Canonical Allele Identifier: CA2466828132
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073022714

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903916dup , CM000685.2:g.154903916dup GRCh38
NC_000023.10:g.154132191dup , CM000685.1:g.154132191dup GRCh37
NC_000023.9:g.153785385dup NCBI36
NG_011403.1:g.123808dup
NG_011403.2:g.123808dup

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5988dup MANE Select ENSP00000353393.4:p.Leu1997SerfsTer7
ENST00000360256.8:c.5988dup ENSP00000353393.4:p.Leu1997SerfsTer7
NM_000132.3:c.5988dup NP_000123.1:p.Leu1997SerfsTer7
XM_011531126.1:c.5883dup XP_011529428.1:p.Leu1962SerfsTer7
NM_000132.4:c.5988dup MANE Select NP_000123.1:p.Leu1997SerfsTer7