Canonical Allele Identifier: CA414910653
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953942G>A , CM000685.2:g.154953942G>A GRCh38
NC_000023.10:g.154182217G>A , CM000685.1:g.154182217G>A GRCh37
NC_000023.9:g.153835411G>A NCBI36
NG_011403.1:g.73782C>T
NG_011403.2:g.73782C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1853C>T MANE Select ENSP00000353393.4:p.Ala618Val
ENST00000647125.1:c.*1729C>T ENSP00000496062.1:n.*1729C>T
ENST00000360256.8:c.1853C>T ENSP00000353393.4:p.Ala618Val
NM_000132.3:c.1853C>T NP_000123.1:p.Ala618Val
XM_011531126.1:c.1748C>T XP_011529428.1:p.Ala583Val
NM_000132.4:c.1853C>T MANE Select NP_000123.1:p.Ala618Val