Canonical Allele Identifier: CA414906050
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903996C>G , CM000685.2:g.154903996C>G GRCh38
NC_000023.10:g.154132271C>G , CM000685.1:g.154132271C>G GRCh37
NC_000023.9:g.153785465C>G NCBI36
NG_011403.1:g.123728G>C
NG_011403.2:g.123728G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5908G>C MANE Select ENSP00000353393.4:p.Glu1970Gln
ENST00000360256.8:c.5908G>C ENSP00000353393.4:p.Glu1970Gln
NM_000132.3:c.5908G>C NP_000123.1:p.Glu1970Gln
XM_011531126.1:c.5803G>C XP_011529428.1:p.Glu1935Gln
NM_000132.4:c.5908G>C MANE Select NP_000123.1:p.Glu1970Gln