Canonical Allele Identifier: CA414920021
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997044G>T , CM000685.2:g.154997044G>T GRCh38
NC_000023.10:g.154225319G>T , CM000685.1:g.154225319G>T GRCh37
NC_000023.9:g.153878513G>T NCBI36
NG_011403.1:g.30680C>A
NG_011403.2:g.30680C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.317C>A MANE Select ENSP00000353393.4:p.Thr106Lys
ENST00000647125.1:c.*103C>A ENSP00000496062.1:n.*103C>A
ENST00000360256.8:c.317C>A ENSP00000353393.4:p.Thr106Lys
ENST00000423959.5:c.212C>A ENSP00000409446.1:p.Thr71Lys
ENST00000453950.1:c.299C>A ENSP00000389153.1:p.Thr100Lys
NM_000132.3:c.317C>A NP_000123.1:p.Thr106Lys
XM_011531126.1:c.212C>A XP_011529428.1:p.Thr71Lys
NM_000132.4:c.317C>A MANE Select NP_000123.1:p.Thr106Lys