Canonical Allele Identifier: CA414919943
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1418523861

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997008T>C , CM000685.2:g.154997008T>C GRCh38
NC_000023.10:g.154225283T>C , CM000685.1:g.154225283T>C GRCh37
NC_000023.9:g.153878477T>C NCBI36
NG_011403.1:g.30716A>G
NG_011403.2:g.30716A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.353A>G MANE Select ENSP00000353393.4:p.His118Arg
ENST00000647125.1:c.*139A>G ENSP00000496062.1:n.*139A>G
ENST00000360256.8:c.353A>G ENSP00000353393.4:p.His118Arg
ENST00000423959.5:c.248A>G ENSP00000409446.1:p.His83Arg
ENST00000453950.1:c.335A>G ENSP00000389153.1:p.His112Arg
NM_000132.3:c.353A>G NP_000123.1:p.His118Arg
XM_011531126.1:c.248A>G XP_011529428.1:p.His83Arg
NM_000132.4:c.353A>G MANE Select NP_000123.1:p.His118Arg