Canonical Allele Identifier: CA414912156
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957129A>C , CM000685.2:g.154957129A>C GRCh38
NC_000023.10:g.154185404A>C , CM000685.1:g.154185404A>C GRCh37
NC_000023.9:g.153838598A>C NCBI36
NG_011403.1:g.70595T>G
NG_011403.2:g.70595T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1580T>G MANE Select ENSP00000353393.4:p.Ile527Arg
ENST00000647125.1:c.*1456T>G ENSP00000496062.1:n.*1456T>G
ENST00000360256.8:c.1580T>G ENSP00000353393.4:p.Ile527Arg
NM_000132.3:c.1580T>G NP_000123.1:p.Ile527Arg
XM_011531126.1:c.1475T>G XP_011529428.1:p.Ile492Arg
NM_000132.4:c.1580T>G MANE Select NP_000123.1:p.Ile527Arg