Canonical Allele Identifier: CA414917707
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969369T>C , CM000685.2:g.154969369T>C GRCh38
NC_000023.10:g.154197644T>C , CM000685.1:g.154197644T>C GRCh37
NC_000023.9:g.153850838T>C NCBI36
NG_011403.1:g.58355A>G
NG_011403.2:g.58355A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.971A>G MANE Select ENSP00000353393.4:p.Gln324Arg
ENST00000647125.1:c.*847A>G ENSP00000496062.1:n.*847A>G
ENST00000360256.8:c.971A>G ENSP00000353393.4:p.Gln324Arg
NM_000132.3:c.971A>G NP_000123.1:p.Gln324Arg
XM_011531126.1:c.866A>G XP_011529428.1:p.Gln289Arg
NM_000132.4:c.971A>G MANE Select NP_000123.1:p.Gln324Arg