Canonical Allele Identifier: CA414906044
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903995T>C , CM000685.2:g.154903995T>C GRCh38
NC_000023.10:g.154132270T>C , CM000685.1:g.154132270T>C GRCh37
NC_000023.9:g.153785464T>C NCBI36
NG_011403.1:g.123729A>G
NG_011403.2:g.123729A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5909A>G MANE Select ENSP00000353393.4:p.Glu1970Gly
ENST00000360256.8:c.5909A>G ENSP00000353393.4:p.Glu1970Gly
NM_000132.3:c.5909A>G NP_000123.1:p.Glu1970Gly
XM_011531126.1:c.5804A>G XP_011529428.1:p.Glu1935Gly
NM_000132.4:c.5909A>G MANE Select NP_000123.1:p.Glu1970Gly