Canonical Allele Identifier: CA414920094
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997076G>C , CM000685.2:g.154997076G>C GRCh38
NC_000023.10:g.154225351G>C , CM000685.1:g.154225351G>C GRCh37
NC_000023.9:g.153878545G>C NCBI36
NG_011403.1:g.30648C>G
NG_011403.2:g.30648C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.285C>G MANE Select ENSP00000353393.4:p.Ile95Met
ENST00000647125.1:c.*71C>G ENSP00000496062.1:n.*71C>G
ENST00000360256.8:c.285C>G ENSP00000353393.4:p.Ile95Met
ENST00000423959.5:c.180C>G ENSP00000409446.1:p.Ile60Met
ENST00000453950.1:c.267C>G ENSP00000389153.1:p.Ile89Met
NM_000132.3:c.285C>G NP_000123.1:p.Ile95Met
XM_011531126.1:c.180C>G XP_011529428.1:p.Ile60Met
NM_000132.4:c.285C>G MANE Select NP_000123.1:p.Ile95Met