Canonical Allele Identifier: CA414920062
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997062T>C , CM000685.2:g.154997062T>C GRCh38
NC_000023.10:g.154225337T>C , CM000685.1:g.154225337T>C GRCh37
NC_000023.9:g.153878531T>C NCBI36
NG_011403.1:g.30662A>G
NG_011403.2:g.30662A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.299A>G MANE Select ENSP00000353393.4:p.Tyr100Cys
ENST00000647125.1:c.*85A>G ENSP00000496062.1:n.*85A>G
ENST00000360256.8:c.299A>G ENSP00000353393.4:p.Tyr100Cys
ENST00000423959.5:c.194A>G ENSP00000409446.1:p.Tyr65Cys
ENST00000453950.1:c.281A>G ENSP00000389153.1:p.Tyr94Cys
NM_000132.3:c.299A>G NP_000123.1:p.Tyr100Cys
XM_011531126.1:c.194A>G XP_011529428.1:p.Tyr65Cys
NM_000132.4:c.299A>G MANE Select NP_000123.1:p.Tyr100Cys