Canonical Allele Identifier: CA2466857776
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997031C= , CM000685.2:g.154997031C= GRCh38
NC_000023.10:g.154225306C= , CM000685.1:g.154225306C= GRCh37
NC_000023.9:g.153878500C= NCBI36
NG_011403.1:g.30693G=
NG_011403.2:g.30693G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.330G= MANE Select ENSP00000353393.4:p.Met110=
ENST00000647125.1:c.*116G= ENSP00000496062.1:n.*116G=
ENST00000360256.8:c.330G= ENSP00000353393.4:p.Met110=
ENST00000423959.5:c.225G= ENSP00000409446.1:p.Met75=
ENST00000453950.1:c.312G= ENSP00000389153.1:p.Met104=
NM_000132.3:c.330G= NP_000123.1:p.Met110=
XM_011531126.1:c.225G= XP_011529428.1:p.Met75=
NM_000132.4:c.330G= MANE Select NP_000123.1:p.Met110=