Canonical Allele Identifier: CA414910658
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1853C>A MANE Select ENSP00000353393.4:p.Ala618Asp
ENST00000647125.1:c.*1729C>A ENSP00000496062.1:n.*1729C>A
ENST00000360256.8:c.1853C>A ENSP00000353393.4:p.Ala618Asp
NM_000132.3:c.1853C>A NP_000123.1:p.Ala618Asp
XM_011531126.1:c.1748C>A XP_011529428.1:p.Ala583Asp
NM_000132.4:c.1853C>A MANE Select NP_000123.1:p.Ala618Asp