Canonical Allele Identifier: CA414917703
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969368C>G , CM000685.2:g.154969368C>G GRCh38
NC_000023.10:g.154197643C>G , CM000685.1:g.154197643C>G GRCh37
NC_000023.9:g.153850837C>G NCBI36
NG_011403.1:g.58356G>C
NG_011403.2:g.58356G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.972G>C MANE Select ENSP00000353393.4:p.Gln324His
ENST00000647125.1:c.*848G>C ENSP00000496062.1:n.*848G>C
ENST00000360256.8:c.972G>C ENSP00000353393.4:p.Gln324His
NM_000132.3:c.972G>C NP_000123.1:p.Gln324His
XM_011531126.1:c.867G>C XP_011529428.1:p.Gln289His
NM_000132.4:c.972G>C MANE Select NP_000123.1:p.Gln324His