Canonical Allele Identifier: CA414919393
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154992950A>C , CM000685.2:g.154992950A>C GRCh38
NC_000023.10:g.154221225A>C , CM000685.1:g.154221225A>C GRCh37
NC_000023.9:g.153874419A>C NCBI36
NG_011403.1:g.34774T>G
NG_011403.2:g.34774T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.587T>G MANE Select ENSP00000353393.4:p.Leu196Arg
ENST00000647125.1:c.*373T>G ENSP00000496062.1:n.*373T>G
ENST00000360256.8:c.587T>G ENSP00000353393.4:p.Leu196Arg
ENST00000423959.5:c.482T>G ENSP00000409446.1:p.Leu161Arg
NM_000132.3:c.587T>G NP_000123.1:p.Leu196Arg
XM_011531126.1:c.482T>G XP_011529428.1:p.Leu161Arg
NM_000132.4:c.587T>G MANE Select NP_000123.1:p.Leu196Arg