Canonical Allele Identifier: CA414917719
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969372C>G , CM000685.2:g.154969372C>G GRCh38
NC_000023.10:g.154197647C>G , CM000685.1:g.154197647C>G GRCh37
NC_000023.9:g.153850841C>G NCBI36
NG_011403.1:g.58352G>C
NG_011403.2:g.58352G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.968G>C MANE Select ENSP00000353393.4:p.Gly323Ala
ENST00000647125.1:c.*844G>C ENSP00000496062.1:n.*844G>C
ENST00000360256.8:c.968G>C ENSP00000353393.4:p.Gly323Ala
NM_000132.3:c.968G>C NP_000123.1:p.Gly323Ala
XM_011531126.1:c.863G>C XP_011529428.1:p.Gly288Ala
NM_000132.4:c.968G>C MANE Select NP_000123.1:p.Gly323Ala