Canonical Allele Identifier: CA414917720
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.968G>T MANE Select ENSP00000353393.4:p.Gly323Val
ENST00000647125.1:c.*844G>T ENSP00000496062.1:n.*844G>T
ENST00000360256.8:c.968G>T ENSP00000353393.4:p.Gly323Val
NM_000132.3:c.968G>T NP_000123.1:p.Gly323Val
XM_011531126.1:c.863G>T XP_011529428.1:p.Gly288Val
NM_000132.4:c.968G>T MANE Select NP_000123.1:p.Gly323Val