Canonical Allele Identifier: CA501127
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs782607735

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969370G>T , CM000685.2:g.154969370G>T GRCh38
NC_000023.10:g.154197645G>T , CM000685.1:g.154197645G>T GRCh37
NC_000023.9:g.153850839G>T NCBI36
NG_011403.1:g.58354C>A
NG_011403.2:g.58354C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.970C>A MANE Select ENSP00000353393.4:p.Gln324Lys
ENST00000647125.1:c.*846C>A ENSP00000496062.1:n.*846C>A
ENST00000360256.8:c.970C>A ENSP00000353393.4:p.Gln324Lys
NM_000132.3:c.970C>A NP_000123.1:p.Gln324Lys
XM_011531126.1:c.865C>A XP_011529428.1:p.Gln289Lys
NM_000132.4:c.970C>A MANE Select NP_000123.1:p.Gln324Lys