Canonical Allele Identifier: CA414919772
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154993118C>T , CM000685.2:g.154993118C>T GRCh38
NC_000023.10:g.154221393C>T , CM000685.1:g.154221393C>T GRCh37
NC_000023.9:g.153874587C>T NCBI36
NG_011403.1:g.34606G>A
NG_011403.2:g.34606G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.419G>A MANE Select ENSP00000353393.4:p.Arg140Lys
ENST00000647125.1:c.*205G>A ENSP00000496062.1:n.*205G>A
ENST00000360256.8:c.419G>A ENSP00000353393.4:p.Arg140Lys
ENST00000423959.5:c.314G>A ENSP00000409446.1:p.Arg105Lys
ENST00000453950.1:c.401G>A ENSP00000389153.1:p.Arg134Lys
NM_000132.3:c.419G>A NP_000123.1:p.Arg140Lys
XM_011531126.1:c.314G>A XP_011529428.1:p.Arg105Lys
NM_000132.4:c.419G>A MANE Select NP_000123.1:p.Arg140Lys