Canonical Allele Identifier: CA414920114
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997087C>G , CM000685.2:g.154997087C>G GRCh38
NC_000023.10:g.154225362C>G , CM000685.1:g.154225362C>G GRCh37
NC_000023.9:g.153878556C>G NCBI36
NG_011403.1:g.30637G>C
NG_011403.2:g.30637G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.274G>C MANE Select ENSP00000353393.4:p.Gly92Arg
ENST00000647125.1:c.*60G>C ENSP00000496062.1:n.*60G>C
ENST00000360256.8:c.274G>C ENSP00000353393.4:p.Gly92Arg
ENST00000423959.5:c.169G>C ENSP00000409446.1:p.Gly57Arg
ENST00000453950.1:c.256G>C ENSP00000389153.1:p.Gly86Arg
NM_000132.3:c.274G>C NP_000123.1:p.Gly92Arg
XM_011531126.1:c.169G>C XP_011529428.1:p.Gly57Arg
NM_000132.4:c.274G>C MANE Select NP_000123.1:p.Gly92Arg