Canonical Allele Identifier: CA414914475
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928788C>T , CM000685.2:g.154928788C>T GRCh38
NC_000023.10:g.154157063C>T , CM000685.1:g.154157063C>T GRCh37
NC_000023.9:g.153810257C>T NCBI36
NG_011403.1:g.98936G>A
NG_011403.2:g.98936G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5002G>A MANE Select ENSP00000353393.4:p.Glu1668Lys
ENST00000360256.8:c.5002G>A ENSP00000353393.4:p.Glu1668Lys
NM_000132.3:c.5002G>A NP_000123.1:p.Glu1668Lys
XM_011531126.1:c.4897G>A XP_011529428.1:p.Glu1633Lys
NM_000132.4:c.5002G>A MANE Select NP_000123.1:p.Glu1668Lys