HGVS | Genome Assembly |
---|---|
NC_000011.10:g.763881A>T , CM000673.2:g.763881A>T | GRCh38 |
NC_000011.9:g.763881A>T , CM000673.1:g.763881A>T | GRCh37 |
NC_000011.8:g.753881A>T | NCBI36 |
NG_008160.1:g.21450A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000319006.8:c.772A>T MANE Select | ENSP00000321259.3:p.Lys258Ter | |
ENST00000319006.7:c.772A>T | ENSP00000321259.3:p.Lys258Ter | |
ENST00000528097.5:c.772A>T | ENSP00000437098.1:p.Lys258Ter | |
NM_006755.1:c.772A>T | NP_006746.1:p.Lys258Ter | |
NM_006755.2:c.772A>T MANE Select | NP_006746.1:p.Lys258Ter |