Canonical Allele Identifier: CA414920011
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997038T>C , CM000685.2:g.154997038T>C GRCh38
NC_000023.10:g.154225313T>C , CM000685.1:g.154225313T>C GRCh37
NC_000023.9:g.153878507T>C NCBI36
NG_011403.1:g.30686A>G
NG_011403.2:g.30686A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.323A>G MANE Select ENSP00000353393.4:p.Lys108Arg
ENST00000647125.1:c.*109A>G ENSP00000496062.1:n.*109A>G
ENST00000360256.8:c.323A>G ENSP00000353393.4:p.Lys108Arg
ENST00000423959.5:c.218A>G ENSP00000409446.1:p.Lys73Arg
ENST00000453950.1:c.305A>G ENSP00000389153.1:p.Lys102Arg
NM_000132.3:c.323A>G NP_000123.1:p.Lys108Arg
XM_011531126.1:c.218A>G XP_011529428.1:p.Lys73Arg
NM_000132.4:c.323A>G MANE Select NP_000123.1:p.Lys108Arg