Canonical Allele Identifier: CA414920116
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997089A>C , CM000685.2:g.154997089A>C GRCh38
NC_000023.10:g.154225364A>C , CM000685.1:g.154225364A>C GRCh37
NC_000023.9:g.153878558A>C NCBI36
NG_011403.1:g.30635T>G
NG_011403.2:g.30635T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.272T>G MANE Select ENSP00000353393.4:p.Leu91Arg
ENST00000647125.1:c.*58T>G ENSP00000496062.1:n.*58T>G
ENST00000360256.8:c.272T>G ENSP00000353393.4:p.Leu91Arg
ENST00000423959.5:c.167T>G ENSP00000409446.1:p.Leu56Arg
ENST00000453950.1:c.254T>G ENSP00000389153.1:p.Leu85Arg
NM_000132.3:c.272T>G NP_000123.1:p.Leu91Arg
XM_011531126.1:c.167T>G XP_011529428.1:p.Leu56Arg
NM_000132.4:c.272T>G MANE Select NP_000123.1:p.Leu91Arg