Canonical Allele Identifier: CA414918398
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969531T>C , CM000685.2:g.154969531T>C GRCh38
NC_000023.10:g.154197806T>C , CM000685.1:g.154197806T>C GRCh37
NC_000023.9:g.153851000T>C NCBI36
NG_011403.1:g.58193A>G
NG_011403.2:g.58193A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.809A>G MANE Select ENSP00000353393.4:p.Lys270Arg
ENST00000647125.1:c.*685A>G ENSP00000496062.1:n.*685A>G
ENST00000360256.8:c.809A>G ENSP00000353393.4:p.Lys270Arg
NM_000132.3:c.809A>G NP_000123.1:p.Lys270Arg
XM_011531126.1:c.704A>G XP_011529428.1:p.Lys235Arg
NM_000132.4:c.809A>G MANE Select NP_000123.1:p.Lys270Arg